Clinical Coord Resume Sample
Waylon Erdman
83699 Fabiola Creek,
San Francisco,
CA
+1 (555) 461 7678
Work Experience
Clinical Rsch Coord., Senior
10/2017
-
PRESENT
Phoenix, AZ
- Possesses strong knowledge base of regulatory standards. Under the direction of Department Director, maintains a state of readiness in accordance with regulations and standards; takes appropriate action to identify and correct gaps
- Screen patients for protocol eligibility through personal interviews and/or medical record review in inpatient and outpatient settings. Identify and meet the educational, emotional, and psychosocial needs of patient and their families while on phase I clinical trials
- Coordinate, evaluate, and follow the patient’s participation in clinical settings. Collaborate with the multidisciplinary team as necessary to document patient care, achieve objectives of phase I trials, and maintain patient safety
- Coordination of regulatory correspondence on clinical research studies
- Complete forms and comply with institutional, state, and federal agencies; prepare reports for the surveillance committee and the sponsoring agencies as specified in the reporting requirements
- Direct support to clinical trial research protocols
- Review protocol documents including abstracts, text and informed consent for relevant information
- Register patients on research protocols by verifying eligibility/exclusion criteria and entering patients in PDMS per protocol. Communicate necessary registration information to sponsoring drug company as directed by PI, and with the assistance of the research nurse
- Assist in the screening for adverse events
Coord, Clinical Studies
04/2012
-
09/2017
Philadelphia, PA
- Knowledge of protocol databases and tools: CRF, CORe, GURU, Microsoft office, Excel, and others as designated
- Consults with PI and the Research Nurse Supervisor (RNS) regarding ongoing study assignments. Collaborates with other members of the multidisciplinary team (research nurses, lab staff, and clinic personnel) as necessary
- Demonstrates proactive and effective oral and written communication skills when contacting other institutions, patients, and agencies (i.e., NCI, pharmaceutical companies, sponsoring agencies, etc.) by phone, email, and/or face to face interactions. Assimilates pertinent information in order to compose written correspondence
- Advocate for the clinical research process per institutional, divisional, and departmental SOPs in keeping with Good Clinical Practice for research
- Assists with the development process of research data management staff
- Experience in the field or in a related area. Familiar with a variety of the field's concepts, practices, and procedures
- Assists in collecting and organizing outside medical records and laboratory results for patients consented on research protocols. Ensures that all the relevant and needed information is available for review and filing. Visually reviews information to be filed in order to classify, file and purge information; scans documents as required
- Assist other staff with organization of research protocols to include ensuring patient folders are complete and available for the research nurse or assist as directed from responsible staff
Asst Clinical Rsch Coord
04/2009
-
11/2011
Phoenix, AZ
- Follow patients while on study for safety monitoring. Adhere to institutional policies concerning safety and infection control
- Provide support for labor-intensive protocols as needed
- Monitor protocol compliance by assisting in coordination of protocol-specific lab, radiographic, and clinical evaluation of patients
- Cover co-workers’ patients as needed
- To assist in the coordination of regulatory correspondence and protocol administration on all departmental clinical research
- In consultation with the physician, assesses patients for eligibility through personal interviews and medical record review. Responsible for accurate and successful patient recruitment to assigned protocols
- Reads protocol and develops systems for screening and scheduling patients. Develops on-study notes and other documents as needed for protocols
- Responsible for accurate and timely transcription of study data to paper and/or electronic Case Report Form (CRF), retrieving information from electronic record, chart, and/or phone call. Requires ability to gather relevant information and determine the appropriate information to report. Responsible for scheduling labs, tracking return visit time points per protocol, tracing and recording
- Responsible for tracking and recording deviations, violations, adverse events and other study related activities
Education
Lawrence University
2003 - 2008
Bachelor's Degree in Biology
Professional Skills
- Strong interpersonal and problem solving skills and an ability to work effectively with others in a team environment
- Strong organizational skills, attention to detail, ability to prioritize and manage multiple tasks, and ability to complete projects under time constraints
- Excellent interpersonal and good presentation skills
- Excellent technical and communication (written and oral) skills necessary
- Excellent organizational/time management skills and close attention to detail
- Excellent interpersonal skills, both in person and over the telephone
- Prior research experience with children, preferably with traumatized populations
How to write Clinical Coord Resume
Clinical Coord role is responsible for research, teaching, development, planning, finance, training, integration, database, procurement, compensation.
To write great resume for clinical coord job, your resume must include:
- Your contact information
- Work experience
- Education
- Skill listing
Contact Information For Clinical Coord Resume
The section contact information is important in your clinical coord resume. The recruiter has to be able to contact you ASAP if they like to offer you the job. This is why you need to provide your:
- First and last name
- Telephone number
Work Experience in Your Clinical Coord Resume
The section work experience is an essential part of your clinical coord resume. It’s the one thing the recruiter really cares about and pays the most attention to.
This section, however, is not just a list of your previous clinical coord responsibilities. It's meant to present you as a wholesome candidate by showcasing your relevant accomplishments and should be tailored specifically to the particular clinical coord position you're applying to.
The work experience section should be the detailed summary of your latest 3 or 4 positions.
Representative Clinical Coord resume experience can include:
- Attends site initiation meetings for relevant studies. Maintains communication with monitors and sponsors regarding the status of patients. Resolves queries and issues related to research protocols
- Coordinate Nursing personnel with patients in order to maximize the skills of the Nurse with the needs of the patients
- Establishes work priorities and daily nursing care assignments in response to patient load
- Recent clinical nursing experience
- Developing supporting materials for Value Analysis Steering Committee meetings, including presentation materials and any required analyses and research
- Manages The Central Staffing Office Personnel To Include Hiring, On-Boarding, Developing, Coaching, Motivating, Evaluating, And Addressing Performance Issues
Education on a Clinical Coord Resume
Make sure to make education a priority on your clinical coord resume. If you’ve been working for a few years and have a few solid positions to show, put your education after your clinical coord experience. For example, if you have a Ph.D in Neuroscience and a Master's in the same sphere, just list your Ph.D. Besides the doctorate, Master’s degrees go next, followed by Bachelor’s and finally, Associate’s degree.
Additional details to include:
- School you graduated from
- Major/ minor
- Year of graduation
- Location of school
These are the four additional pieces of information you should mention when listing your education on your resume.
Professional Skills in Clinical Coord Resume
When listing skills on your clinical coord resume, remember always to be honest about your level of ability. Include the Skills section after experience.
Present the most important skills in your resume, there's a list of typical clinical coord skills:
- Experience: Three years experience as a registered nurse
- Experience conducting developmental, psychological or academic tests on infants and young children
- Recent clinical nursing experience is required
- Demonstrated working knowledge and completion of MGH research educational requirements (CITI and Human Studies)
- Experience in functional magnetic resonance imaging (2 years)
- Experience in utilizing statistical methods to analyze combined fMRI, psychophysiological and serology data
List of Typical Experience For a Clinical Coord Resume
1
Experience For Clinical Rsch Coord., Senior Resume
- Manages research charts and assist research nurse with preparation for monitoring/auditing
- Assists with scheduling procedures for patient appointments
- Supports grant management responsibilities for unit, including the development of study budgets
- Meet weekly with PI and staff to review protocol activities. Prepares reports as needed for primary investigator
- Consents patients for other correlative lab studies; documents process accordingly. Notifies appropriate parties of patient registrations
- Administers required surveys and reviews for completeness
- Registers patients into CORe / Epic
2
Experience For Coord, Clinical Studies Resume
- Enters patient orders and treatment plans appropriately, links all research activities to the research study
- Screen patients for protocol eligibility through personal interviews and/or medical record review in inpatient and outpatient settings. Identify and meet the educational, emotional, and psychosocial needs of patient and their families while on clinical trials
- Coordinate, evaluate, and follow the patient’s participation in clinical settings. Collaborate with the multidisciplinary team as necessary to document patient care, achieve objectives of clinical research trials, and maintain patient safety
- Verify inclusion and exclusion criteria by reviewing medical records and interviewing the patient
- Register patients on clinical trial following requirements of protocol. Register patients in CORe
- Oversees and coordinates audit activities as needed
- Read, interpret, and process large quantities of printed information
3
Experience For Senior Coord, Clinical Studies Resume
- Be clearly understood by verbal communication in face-to-face encounters and by telephone, read printed and written data, assimilate pertinent information in order to compose written correspondence
- Engage in a variety of telephone and face-to-face meetings related to pending and active projects on a daily basis. Respond and assist other employees and visitors, as required
- Compare database and file material on an ongoing basis
- Organize focus on task is essential
- Build and/or maintain simple Excel spreadsheets. Manually record data, by use of a computer and keyboard
- Records adverse events for Research Nurses/Principle Investigators review. Records and submits internal and external severe adverse events
- Assists preparation of protocol annual review
- Assesses patients and provides logistical details of protocol to patients at the clinic when needs present
- Demonstrates excellent oral and written communication skills when contacting other institutions and agencies by phone, computer-generated reports and/or face to face contacts
4
Experience For Asst Clinical Rsch Coord Resume
- Able to review eligibility of potential patients and provide study specific pertinent information to physicians, nurses and patient-care givers to facilitate prompt and precise enrollment of patients in protocols. Able to register patients on protocols by computer via keyboard or by telephone
- Assists with statistical analysis of research studies by computer via keyboard or by using a hand held calculator as well as hand written charts and notes
- Assists in retrieval of pathology slides/blocks and mail as specified in protocols
- Assists research nurses with “long term” follow up clinical appointments
- Assists the faculty investigator in the overall conduct of the clinical trials assigned maintaining adherence to the protocol. Contributes in the department of ID/IC/EH protocol review and submission process and attend protocols meetings
- Spends 50% or more time in direct patient contact. Obtains consenting for minimal risk studies. Follows-up protocol submission about research investigations, laboratory tests and responses
- Assists the faculty investigator in data file preparation and attends data review meetings as required by the department. Prepares specific protocol reports and analysis and assist in manuscript preparation and grant submissions
5
Experience For Clinical Rsch Coord Assoc Resume
- Participates and ensures prospective data collection is entered in a timely manner into the departmental database and/or study CRF/eCRF
- Attends departmental meetings as required. Attends research team meetings
- Attends planning clinics and meetings as required. Maintains contact with other institutions in studies. Interacts with members of interdisciplinary team inter and intra-departmentally to request information and verify the status of ongoing projects. Assists the PI in monitoring progress of project work
- Searches and reviews literature in pertinent areas, preparing written reports as necessary. Organizes and maintains copies of journal articles. Creates and organizes grant material, manuscripts, bibliographies, literature, abstracts, tables, figures, conference materials, etc
- Label and record biological specimens to enter into a database. Coordinate receipt and delivery to appropriate laboratories. Orders and stocks supplies in support of study needs
- Performs analysis of data. Uses ancillary software (Excel, Access, SPSS, etc.) to analyze or interpret data and generate data files or reports in the format requested by the PI
- Assists the PI in the development, writing, and submission of new protocols to the IRB, as well as manages the resubmission of any amendments to active protocols, as necessary
- Register patients on research protocols by verifying eligibility/exclusion criteria and entering patients and data into required database (per protocol)
6
Experience For Clinical Transplant Coord Resume
- Communicate necessary registration information to the department personnel and the sponsoring drug company as directed by the PI
- Help to gather literature, integrate literature, and write research proposals for potential pharmaceutical company sponsored projects
- Train new hires in study coordination to include providing training and guidance with regard to the policies and procedures related to clinical trials. Assists in the management of other assistants and volunteers who also work for the PI to ensure accurate data collection, appropriate work delegation, etc
- Coordination and oversight of activities related to initiation and conduct of Strategic Alliance clinical trials
- Coordinate, evaluate, and follow the patient’s participation in clinical settings. Provide collaborative oversight for the multidisciplinary team as necessary to document patient care, achieve objectives of clinical trials, and maintain patient safety
7
Experience For Clinical Rsch Coord Resume
- Understand and adhere to policies and procedures related to conduct of clinical trials
- Provide leadership for the overall effective operation of designated protocols, which includes development, design, and resolution of operations and issues in collaboration with the DoCM team, Strategic Industry Ventures team, central office personnel, principal investigator and/or study sponsor
- Act as liaison with patients, physicians and research staff in providing administrative and patient care services for the coordination of research studies
- As applicable to clinical activities, complete case report forms in a timely and accurate fashion
- Understand and adhere to policies and procedures related to safety, infection control and conduct of clinical trials
8
Experience For Coord Clinical Coord Ctr Resume
- Oversee, coordinate, and participate in the collection and evaluation of data for principal investigators
- Monitor the retrieval of protocol-related data as documented in the medical record and ensure accurate entry into computerized database
- Generate data reports, protocol summary reports, and user-generated data reports as requested
- Assist upon request with preparation of technical reports, abstracts, posters and manuscripts
- Train and mentor new study coordinators and data coordinators to perform the functions delineated in their position descriptions
- Provide input for performance evaluations
- Ensures adequate coverage for all positions within the department
- Contacts private Physicians when needed
- Contributes input for the department and implementation of department policies and procedures. Interprets and instructs subordinate personnel on policies and procedures and assures proper compliance
9
Experience For Clinical Trials Coord B Resume
- Ensures that all patient personal belongings and valuables are tagged and taken to the appropriate area
- Maintains adequate levels of approved supplies and equipment, i.e. stock medications, pharmacy supplies and oxygen tanks to perform immediate emergency care; ensures count for narcotics are accurate
- Establishes and maintains a cooperative working relationship with various departments to secure accommodations and request needed services
- Ensures proper use, repair, and replacement of departmental equipment and supplies; makes necessary arrangements for repairs and/or maintenance of department equipment and facilities in the absence of the Supplies Coordinator
- Prepares and submits incident reports on unusual occurrences or incidents
- Promotes good public relations through positive interactions with patients, family, visitors, Physicians, police, press, ambulance personnel and other Hospital personnel
- Serves on committees, attend meetings and educational seminars to enhance and maintain awareness in Nursing techniques and procedures
10
Experience For Clinical Coord Tri Cities Free Standing ER Resume
- Assumes that all treatments and procedures are carried out as ordered
- Is aware of all patients signing in to be treated and assures that needed care is being performed expeditiously; Is aware of condition of all unstable patients and assures that their condition is being monitored properly; and Is aware of patient flow in the Emergency Department and takes necessary action to resolve problems if they develop
- Holds team conference/in-service as the need arises
- Monitors all activities of staff
- Assures that all operational policies/procedures of the Emergency Department are adhered to
- Assists and performs functions of a Staff Nurse care as time permits
- Schedule and/or call subjects for appointments; contact participants with reminders or other requirements. Arrange specimen pick-up schedule and coordinates with Courier
List of Typical Skills For a Clinical Coord Resume
1
Skills For Clinical Rsch Coord., Senior Resume
- Previous experience with sample collection processing
- Demonstrates and promotes hospital and nursing Mission, Vision, Philosophy and Core Values
- Two or more years experience in a Clinical Environment required
- Research experience, particularly with patients with Alzheimers or related disorders
- Make independent, effective decisions
2
Skills For Coord, Clinical Studies Resume
- Demonstrate respect and professionalism for subjects’ rights and individual needs
- Experience with diabetes research desired
- Experience in a clinical or research environment as a student, intern, or employee
- Demonstrated interest in maternal and child health
- Experience with project management or coordination
- Experience with University-related research policies and procedures
- Identify problems and develop effective solutions
3
Skills For Senior Coord, Clinical Studies Resume
- Understanding of lab protocols
- Maintain a satisfactory work environment by organizing and redistributing files, records, etc., requiring bending, stooping, reaching, lifting, etc
- Advises and/or assists clinical investigators with initiating and developing clinical trial concepts, including protocol design and protocol writing
- Provide leadership in determining, recommending, and implementing improvements to policies/processes; define best practices
- Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies
- Accountable For The Further Development And Assisting Others In Applying Ndnqi In Their Leadership Practice
- Assists in designing and implementing quality assurance systems to assure compliance
4
Skills For Asst Clinical Rsch Coord Resume
- With the Grant Manager and study staff, assists with the budgeting and monitoring of NeuroNext grant and study funds
- Schedule, or assist with scheduling, screening assessments
- Schedules assignment, assists with orientation, training, evaluations, and counseling of all subordinate personnel
- Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping
- Previous knowledge of Stanford systems including Epic (medical record system) and eprotocol for human subjects protocols
- Graduate of a Baccalaureate nursing program
5
Skills For Clinical Rsch Coord Assoc Resume
- Previous knowledge of Stanford systems including Epic (medical record system) and e-protocol for human subjects protocols
- Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct
- Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements
- Comfort working with diverse populations
- Research information as requested by Non-Clinical Collaborative Teams and the Value Analysis Steering Committee and provide assistance when needed
- Assist with training of CRC I’s, as needed
- Coordinate completion by students of all clinical competencies, and ensures all of the objectives are met during the duration of the clinical rotation
- Assists investigators in grant writing preparation. Reviews and edits materials for grant submission or publication and/or presentation as needed
6
Skills For Clinical Transplant Coord Resume
- Monitors and ensures compliance of all clinical researchers and their research teams with NIH and MGH required human subjects protection training
- Directly coordinates NeuroNEXT studies when necessary inc. regulatory documentation, screening, recruitment and execution of study procedures
- Organizes and implements Harvard Partners NeuroNext operational meetings, training seminars, and study-specific team meetings
- Create standard operating procedures for the unit
- Communicate necessary registration information to sponsoring drug company as directed by PI, and with the assistance of the research nurse
- Assist in assessing for adverse events
- Travel to and from different destinations, including inpatient and outpatient care areas
7
Skills For Clinical Rsch Coord Resume
- Reads and becomes familiar with protocol specific guidelines and general procedures for caring for the protocol related patients
- Verifies, enters and maintains information in computer database via computer and/or by writing by hand on case report forms
- Work with PI and Physicians in referring departments to identify potential patients for studies
- Participate in maintaining data necessary for audits and assists with audit responses as requested
- Assist with supervisory functions such as counseling employee in regard to institutional policies and procedures
- Provide training and guidance with regard to policies and procedures that are related to conduct of clinical trials
8
Skills For Coord Clinical Coord Ctr Resume
- Monitor accuracy compliance by study coordinators and data coordinators by performing QA audits
- Conduct department training sessions to insure protocol compliance and dissemination of new information and policies
- Supervises subordinates to ensure nursing care is administered in accordance with established standards
- Proficiency with Microsoft Office and database applications
- Work independently and as a team player with very little general direction from the PI or Department Administrator
- Perform basic measurements and tests on patients according to protocol, such as obtaining vital signs and performing phlebotomy and EKG, after appropriate training/certification. Collect study specimens according to protocol. - NA
- Prepare, process, and ship specimens/samples accurately under well-defined requirements.-NA
- Order and maintain equipment and supplies.-NA
- BA/BS in Psychology, Education, Social work or related field of study
9
Skills For Clinical Trials Coord B Resume
- Certified Clinical Transplant Coordinator
- Current Pennsylvania licensure or eligible for Pennsylvania licensure as a Registered Professional Nurse
- Current certification as a Clinical Transplant Coordinator (CCTC) by the American Board for Transplant Certification (ABTC) for a Clinical Transplant Coordinator II
- Knowledge of Baxter products and competitive products is helpful
- Knowledge of clinical processes is highly desired
- Graduation from an accredited program recognized by the Commission on Accreditation of Allied Health Education Programs
- Registry/certification in echocardiography, abdomen, and OB/GYN is required
- Familiarity with tablet technology and mobile application
- Work independently and follow protocols when necessary
10
Skills For Clinical Coord Tri Cities Free Standing ER Resume
- Collaborate with stakeholders from various disciplines and research subjects
- Lead others, take initiative and think independently are also required
- Neonatal Resuscitation required within thirty days of hire
- Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out
- Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms
- Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed
- Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact
- Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff
- Participate in monitor visits and regulatory audits
List of Typical Responsibilities For a Clinical Coord Resume
1
Responsibilities For Clinical Rsch Coord., Senior Resume
- Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to gather data, as needed
- Recent (within 5 years of hire date) transplant experience required
- Operate standard office technology (fax, scanner, multi-line phone Basic knowledge of Microsoft Office
- Collaborates with patients, families, and the healthcare team to coordinate care for an effective and current plan of care
- Managing the operation of study visits and serves as liaison to study participants on scheduling and study-related questions
- Responsible for conducting physiologic tasks, neuroimaging and administrative work associated with running the study
2
Responsibilities For Coord, Clinical Studies Resume
- Coordinates lab activities and performs study procedures such as EKGs and vitals and assisting with phlebotomy
- Interaction with a large team of study staff, including physicians, microbiologists, and laboratory scientists
- Improvement Activities And Related Decisions Are Inclusive Reflecting The Voice And Efforts Of Individuals Throughout Pcs Who Are Impacted In Change Efforts
- Currently licensed as a Registered Nurse, in the State of Virginia or awaiting reciprocity
- Coordinates and/or participates in reviewing all newly diagnosed breast cancer cases and current treatment protocols
- Extract data from source documents for research studies as directed. Collect data and complete case report forms
- Prepare, process, and ship specimens/samples accurately under well-defined requirements
- Perform initial conflict of interest searches and report potential violations to VP of Value Analysis
- Tracks Dr. Purdon’s trainees and postdocs, and coordinate onboarding and orientation of new students, employees, and fellows, including management of visa paperwork processing at the Partner’s International Office
3
Responsibilities For Senior Coord, Clinical Studies Resume
- Maintain Dr. Purdon’s CV, online profiles, and biographies, lab websites
- Establish procedures, guidelines, clinical policies and procedures, and handbooks for the clinical education component of the curriculum
- Schedule students for clinical rotations and coordinate the schedule among clinical affiliates
- Make periodic visits to affiliated organizations to meet with the clinical faculty and student interns for the purpose of
- Serves as a central research resource for all clinical investigators
- Assists in maintenance and organization of active protocol list
- Advises and/or assists on completing relevant paperwork (along with departmental grants administrators) to facilitate transfer of data and/or specimens for research purposes (Data Use Agreements and Material Transfer Agreements)
- Maintains a good working knowledge of applicable institutional guidelines for proper research conduct, Code of Federal Regulations, International Code of Harmonization Guidelines, and State regulations
4
Responsibilities For Asst Clinical Rsch Coord Resume
- Collaborates with the CCPO to ensure timely submission and processing of clinical trial protocols, and timely response to IRB/SRC queries by the investigative team
- Responsible for the day-to-day development, implementation, and analysis of the Lurie Center for Autism research initiatives
- Develops and implements recruitment strategies and is able to independently judge suitability of research subjects
- Collects & organizes patient data, organizes and interprets data; obtains patient study data from medical records, physicians, etc
- Verifies accuracy of study forms and updates study forms per protocol
- Verifies subject inclusion/exclusion criteria and confirms subject meets criteria
- Collects specimens. Labels and completes lab requisitions, including ICD and CPT coding. Sends specimens to lab per patient’s insurance plan. Performs reconciliation of labs and orders and independently follows-up on overdue pending results
5
Responsibilities For Clinical Rsch Coord Assoc Resume
- PERI-OPERATIVE PERIOD - Reviews potential recipient's current medical and financial status to determine eligibility for transplant. - Coordinates admission or transfer to UPMC. - Communicates with organ procurement agency/ORC and collects the appropriate data necessary for decision making re: organ acceptance/rejection for transplant
- POST-TRANSPLANT IN-PATIENT PERIOD - Monitors patient progress post-transplant and educates recipient/family regarding care and responsibilities after transplantation. - Collaborates with transplant team to establish and implement patient plan of care
- PROFESSIONAL GROWTH AND DEVELOPMENT - Obtains ABTC Certification within 2 years. - Takes action to improve knoweldge, skills and performance based on feedback or on self-identified developmental needs. This includes attending practice-related conferences, participating in educational and outreach activities, etc
- Demonstrates Energized Project Leadership In Order To Inspire Confidence And Motivation Among Stakeholders
- Service ? Demonstrate Commitment To Service And Contribute To Creating A Positive, Caring Environment
- Assist with training of CRC I’s and II’s, as needed
- Assistance with maintaining a website that hosts the above-referenced health materials
- Preparation of written health materials for international travelers and practitioners
- Support for the prospective observational study of acquisition of antimicrobial-resistant organisms by international travelers, including preparing study materials, enrolling travelers, contacting travelers in follow-up, maintaining database, and overseeing sample storage
6
Responsibilities For Clinical Transplant Coord Resume
- Design research protocols in conjunction with the PI
- Challenges Traditional Practices In Pcs In Order To Explore Innovative Possibilities And Mine For Fresh Ideas. Stimulates Creativity In Other Stakeholders
- Manages And Assists Others In Managing, Multiple Demands And Competing Priorities As They Relate To Process/Performance Improvement Activities And Daily Operations
- Excellence ? Strive For Excellence By Building Upon Past Accomplishments And Strive To Achieve Higher Levels Of Success
- Guest Relations ? Responsible For Courteously Providing Efficient, Friendly Customer Service To All Patients And Co-Workers With Respect And Dignity
- Respect ? Recognize And Value The Unique Contribution Of Each Team Member
7
Responsibilities For Clinical Rsch Coord Resume
- Teamwork ?Participate As A Team Member To Meet The Department / Hospital Objectives. Team Building Includes Cooperation, Willingness To Assist Fellow Employees, Flexibility, Positive Attitude, And Seek Peer Input For Problem Solving. Working Together Sets Us Apart From The Rest
- Understands And Applies Contractual Requirements And Promotes Positive Labor Relations While Advancing The Needs Of The Organization
- With general direction from Senior Program Manager and the NeuroNEXT PI , oversees study operations for all NeuroNext studies
- Coordinates efforts for all NeuroNext studies and provides guidance to the study specific staff in protocol implementation, meeting recruitment goals, performing clinical procedures and managing data collection
- Establishes recruitment strategies and assures implementation and goal attainment on NeuroNext trials and other NINDS funded research
- Monitors study performance for subject accession and data acquisition in accordance with the protocols and conveys information to NeuroNext PIs
- Serves as resource for all regulatory and operational aspects of the Harvard Partners NeuroNext site, overseeing submission and maintenance of documentation to the IRB and sponsors
- Interacts directly with study sponsors, the NIH, other clinical sites, the Clinical Coordination Center, and the Data Coordination Center; Is responsible for assuring that study data is communicated in a timely fashion including study data points, screening and enrollment information, and adverse events, as required per protocol
- Ensures compliance with applicable NeuroNext, FDA, NIH and other regulatory agencies’ requirements
8
Responsibilities For Coord Clinical Coord Ctr Resume
- Schedule and/or call subjects for appointments; contact participants with reminders or other requirements
- Review medical records and/or perform telephone or in-person interviews to gather data, as needed
- Administer standard study questionnaires and tests, score test measurements and questionnaires, and code data for computer entry. Perform quantitative review of forms, tests, and other measurements for completeness and accuracy
- Perform basic measurements and tests on patients according to protocol, such as obtaining vital signs and EKG, after appropriate training
- Coordinate collection of biospecimens in cooperation with phlebotomists and laboratory processing technicians. Biospecimens include: blood, saliva, stool, urine, buccal swab, skin swab, tears, etc
9
Responsibilities For Clinical Trials Coord B Resume
- Liaise with research participants during study visits
- Maintain a variety of complex records; suggest or make improvements to record-keeping procedures
- Coordinate specimen shipment accurately under well-defined requirements
- Documents action taken (services rendered, cancelled, etc.) in patient’s medical record
- Communicates professionally with other team members and colleagues by following approved methods of communication as applicable (I Care, Scripting, SBAR, Huddles, and Bedside Reporting, Leader Rounding)
- Work requires knowledge of operation of department patient care techniques and methods. Possesses knowledge generally
- Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials
10
Responsibilities For Clinical Coord Tri Cities Free Standing ER Resume
- Oversee data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data
- Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance
- Develop project schedules, targets, measurements, and accountabilities, as assigned. Lead team meetings and prepare/approve minutes
- Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to requests and questions
- Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries
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Work Experience
• Coordinates the processing of ARAMARK’s vendor service contracts from field inception through approvals, purchase order release, annual renewals and expirations
• Establishes or ensures the establishment of work priorities and provides daily supervision and support to all assigned staff
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Professional Skills
• Strong organizational skills, attention to...
• Excellent verbal, written and communicatio...
• Excellent verbal, written & communication ...