Associate / Medical Director Resume Sample

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Diamond Sawayn
84958 Romaguera Forks,  Phoenix, AZ
+1 (555) 429 5457

Work Experience

Associate Medical Director / Medical Director
12/2015 - PRESENT
Los Angeles, CA
  • Primarily serves as Global Medical Advisor on assigned projects
  • Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects
  • Ensure that the knowledge and skills of Region 4 colleagues as well as Jazz’s external partners, with respect to Jazz Pharmaceuticals’ products and the appropriate therapy area, are at the highest level
  • Set SMART objectives and track, measure and report progress of plans and budgets
  • Systems, Processes and Ways of Working
  • Expert scientific knowledge of appropriate Region 4 team members as well as Jazz’s external partners for the region
  • Appropriate positioning of Jazz Pharmaceutical medicines in medical guidelines
  • Review and approval of medical and marketing materials and activities in line with national regulations
Associate Medical Director, Partner Markets
08/2012 - 10/2015
New York, NY
  • Attend appropriate scientific congresses to stay abreast of developments and to support Regional and National KOL activities
  • Develop depth of understanding for assigned products, related medical areas, and competitors on an ongoing basis
  • Critically review content developed by others in the agency, including copywriters, medical writers, and AMDs
  • Provide exceptional scientific expertise and collaboration within the Ocrelizumab medical team, to your peers within Neuroscience Group and to the organization in general
  • Build excellent relationships and interactions between Medical and Global functions
  • Contribute to the formation, refinement and execution of medical strategies and tactics including Phase IIIb/IV activities, safety adjudication and exploratory data analysis
  • Ensure strategic partnerships with key opinion leaders in the area of multiple sclerosis patient groups and scientific institutions and societies to enable optimal collaboration for medical products throughout their lifecycle
National Associate Medical Director
05/2008 - 02/2012
Dallas, TX
  • Contribute and provide expert review of medical content for Medical Information and Educational activities
  • Ensure medical and product information is provided in compliance with Global and Genentech SOPs and that all data used in the provision of Medical information are accurate and meet the needs of internal and external customers
  • Contribute to the development of a strategic and robust Medical Advisory Board plan that aims to enhance product knowledge and to inform on clinical practice patterns and gaps
  • Provide leadership and guidance to Clinical trial activities conducted as part of Medical Affairs and provide medical oversight of the safety of local clinical activities
  • Ensure optimal investigators selection by a constructive dialogue between medical and clinical operations
  • Ensure medical review and approval of all promotional materials in compliance with Codes of Practice, Genentech SOPs, and US regulations
  • Verify the accuracy of training material for scientific and product information and drug safety reporting requirements to the local organization (including the sales force)


Lawrence University
2003 - 2007
Science's Degree in Business

Professional Skills

  • Exhibit leadership skills within and outside of the organization (including people skills, mentoring, presentation skills and professional interaction)
  • Team player and strong teambuilding skills
  • Excellent telephonic and interpersonal communication skills
  • Experience of supervising collaborating with Patient Safety colleagues (scientists, product managers, etc)
  • Act as an agent for change when new projects are launched or priorities change by creating and communicating value proposition or business rationale
  • Experience working with the principles and techniques of data analysis, interpretation and clinical relevance (e.g., ISS,ISE, competitor data, etc.)
  • Demonstrate willingness to work beyond basic responsibilities to assist team

How to write Associate / Medical Director Resume

Associate / Medical Director role is responsible for organization, travel, research, design, reporting, oncology, training, health, leadership, landscape.
To write great resume for associate / medical director job, your resume must include:

  • Your contact information
  • Work experience
  • Education
  • Skill listing

Contact Information For Associate / Medical Director Resume

The section contact information is important in your associate / medical director 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
  • Email
  • Telephone number

Work Experience in Your Associate / Medical Director Resume

The section work experience is an essential part of your associate / medical director 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 associate / medical director responsibilities. It's meant to present you as a wholesome candidate by showcasing your relevant accomplishments and should be tailored specifically to the particular associate / medical director position you're applying to. The work experience section should be the detailed summary of your latest 3 or 4 positions. Representative Associate / Medical Director resume experience can include:

  • Forge strong relationships with key opinion leaders
  • Pharmacovigilance experience
  • Pharma/biotech industry experience OR is a recognized expert in the field
  • Experience with clinical trials across Phase I - II - III drug development
  • Answering day to day medical and scientific questions, provide daily medical support to PAREXEL staff or site (investigator/study coordinator)
  • Medically qualified with completion of training in a clinical setting (internship, residency etc)

Education on an Associate / Medical Director Resume

Make sure to make education a priority on your associate / medical director resume. If you’ve been working for a few years and have a few solid positions to show, put your education after your associate / medical director 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 Associate / Medical Director Resume

When listing skills on your associate / medical director 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 associate / medical director skills:

  • Solid tumor experience, preferably in Breast and/or GI Cancer, as well as experience in or exposure to Cancer Immunotherapy
  • For Medical Directors: 3 to 6 years of industry experience; For Associate Medical Directors: 2 to 3 years of industry experience
  • An excellent scientific track record demonstrated by publication record in peer-reviewed journals
  • A demonstrated ability to understand clinical practice, standards of care and epidemiological data in the USA
  • Haematology/oncology experience a distinct advantage
  • M.D. Pediatric Oncologist with relevant medical experience required

List of Typical Skills For an Associate / Medical Director Resume


Skills For Associate Medical Director / Medical Director Resume

  • Think creatively and efficiently to define problems, collect data, establish facts and draw valid conclusions
  • Experience in clinical practice, with a specialty in Oncology
  • Experience in Clinical Research/Pharmaceutical medicine desirable but not essential
  • Monitor and identify relevant literature and craft marketing implications for brand
  • EU - registered to practice in the EU
  • Begin to interact with internal teams, clients, and HCPs on programs to meet strategic objectives through advocacy development, use of medical marketing rationale, and identification/selection of appropriate HCPs
  • Participate in proprietary workshops

Skills For Associate Medical Director, Partner Markets Resume

  • Establish rapport with client and manage medically-related client interactions unsupervised once training is complete and supervisor has adequately modeled appropriate client interactions
  • Develop presentation skills; begin to clearly communicate medical concepts in a condensed, audience-appropriate way to client and agency
  • Residency or fellowship training in Medical oncology, immuno-oncology or Internal medicine. (Not mandatory but highly desirable)
  • MSc/PhD in scientific discipline with ability to analyze and present scientific safety data to different functional areas / audiences
  • Complete timesheets accurately and on time
  • Develop ability to reasonably estimate hours required to complete specific projects
  • Excellent project management skills, good interpersonal, verbal communication and influencing skills, works well within teams and is effective in collaborating with others internally and externally
  • Run a clinical research study with appropriate supervision

Skills For EU / ROW Associate Medical Director Resume

  • Sound knowledge of the managed care industry
  • MD, PhD, PharmD or DO
  • Proven leadership experience and able to work both independently and as a member of an integrated, interdisciplinary team in carrying out assigned responsibilities
  • Track record of forming compliant partnerships with commercial colleagues
  • Significant successful interactions with key opinion leaders and investigators
  • Ensures provision of direct medical services to patients either directly or through arrangements, as appropriate in the absence of the patient’s attending physician

Skills For National Associate Medical Director Resume

  • Contribute to and review clinical documents (slide presentations, protocols, clinical study reports, regulatory submission sections, investigator ’ s brochures, etc.)
  • Participates in the preparation of regulatory documents in support of regulatory submissions, including clinical section of IND’s and CTA’s, IND safety reports and annual reports for assigned trials, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate
  • Acts as liaison between Clinical Development and other internal groups at Vertex (e.g., Regulatory Affairs, Clinical Development Execution) for assigned studies
  • Contribute to the development of and maintain awareness of the competitive landscape and communicate intelligence to the medical and marketing team as appropriate
  • Deliver non-promotional clinical/scientific presentations relating to Jazz’s portfolio and its development or differentiation as required
  • Support the approval and implementation of these projects in line with relevant pharmaceutical regulations and Jazz SOPs as appropriate
  • Stays abreast of professional information and technology through conferences, medical literature, and other available training, to augment expertise in the therapeutic area
  • Understand assigned products’ pharmacology and mechanism of action from a safety perspective, relevant nonclinical toxicology data and clinical AE profile

Skills For Associate Medical Director Physician Resume

  • Provide leadership and support for the development and implementation of a cohesive approach to measuring and promoting quality and support priority-setting process for clinical quality improvement for MassHealth’s payment and care delivery innovation initiatives, including ACOs and CPs
  • Ensure that the strategic positioning is in line with company goals and anticipate and plan for problems/challenges and establish contingency plans and course corrections
  • Oversee quality, coordination and timeless of clinical sections of IND’s, Investigator Brochures, CTA’s , ISS’, ISE’s and clinical expert reports
  • Oversee quality, coordination and timeless of clinical sections of IND’s, Investigator Brochures, CTA’s, ISS, ISE’s and clinical expert reports
  • The ability to think globally, strategically and innovatively about the future of the disease state and company’s therapeutic agents and possess a solid understanding of the pharmaceutical industry, company competition
  • Lead and participate in ongoing CST and relevant sub-team meetings, other interactions and communications
  • Provide scientific and medical leadership as needed for publication planning and execution
  • Participate in Clinical Development strategy development and presents to various internal committees

Skills For Associate Medical Director, Benefit Resume

  • Provide clinical oversight across all relevant studies and programs
  • Work with regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation. Support other functions and teams with clinical science information and input for regulatory submissions and other regulatory processes. Includes developing labeling and packaging language, etc
  • Play a lead role in the development and implementation of communications strategies to support existing and concluded studies. Includes KOL interactions, advisory boards, major medical meetings, congresses and other events, publications and other materials
  • Contribute clinical science input into the relevant therapeutic/disease area scientific strategy. Help Research and other PD groups to ensure consistency of scientific and late-development strategies with target label claims and corporate goals
  • Provide medical expertise to the Commercial organization to compliantly assist in the development and execution of Commercial activities

Skills For Associate Medical Director, Oncology Resume

  • Serve as medical affairs reviewer for promotional materials and non-promotional scientific materials
  • Work with strategic alliances and partnerships as needed
  • Review Investigator Sponsored Study proposals
  • Provide support for Medical Science Liaison activities
  • Provide support as needed to Clinical Development and Clinical Operations to ensure successful execution of our clinical trials program
  • Support high-quality execution of corporate-wide initiatives
  • Basic or clinical research experience in an academic or industrial setting, with experience in analysis of research data and publications; working knowledge of biostatistics and pharmacokinetics; working knowledge of GCP, scientific and clinical research methods and clinical study design

Skills For Associate Medical Director ACH Pediatric Resume

  • Clinical practice (any setting) and experience working with post-registration assessment / evaluation of safety and or efficacy as well as FDA regulatory reporting requirements
  • Up to 3 years of Medical Research, Drug Development, or Patient Safety experience with clear evidence of delivery
  • Provide input as necessary to Feasibility Studies, Data Monitoring Committees (DMCs), Clinical Endpoint Committees (CECs)
  • Maintain up-to-date knowledge of therapeutic area expertise by attending Professional Society Meetings
  • Provide medical expertise and training to other PAREXEL personnel, as required
  • Represent GNE Neuroscience Med Affairs externally through presentations at key National / International meetings, interactions with our key investigators
  • Provide support in preparation of Periodic Safety Update Reports (PSURs)

Skills For Associate Medical Director, Clinical R & D Resume

  • Review and sign off technical documents written by PAREXEL with respect to medically relevant matters with particular attention to those relating to drug safety
  • Provide support for the preparation of clinical protocols, integrated clinical and statistical summary reports, journal articles, and other documents for clients/sponsors in conjunction with clients/sponsors or in conjunction with other PAREXEL departments
  • Attend and present material (such as therapeutic area training) as requested, at internal and external meetings (e.g. investigator meetings)
  • Provide medical expertise to client as contracted
  • With appropriate supervision, manages the design and implementation of study protocols for a clinical development program in support of the overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations and emerging issues
  • The ability to think globally, strategically and innovatively about the future of the disease state and company’s therapeutic agents and possess a solid understanding of the pharmaceutical industry, company competition and commercial side of business, including Marketing and Sales, Market Access, Pricing/Reimbursement, Business Development, Medical Affairs and Supply Chain
  • Review and sign off adverse events reports for accuracy and clinical importance, relationship to the study drug as well as for severity and seriousness; provide reports to European Regulatory Authorities, FDA or other regulatory agencies; provide sponsors with periodic experience reports summarizing adverse events as required by the sponsor or authorities
  • Review and sign off Data Management listings of safety data(including adverse events, laboratory data, vital signs data, medical history, physical examination, concomitant medication), establish the presence or absence of clinically meaningful trends and, if noted, follow up as appropriate with the project team, sponsor, investigator, and Regulatory Authorities

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