The main duty of an Associate Medical Director is to oversee the administration of patient care and take responsibility for implementing and monitoring the integrated clinical practice delivery models. While duties vary based on the requirements of the facility, the following are certain core duties identified on the Associate Medical Director Resume – supervising physicians and collaborating with other clinical managers, providing and managing direct health care for the specified patient population, maintaining patient care protocol and standards, participating in implementation and development of policies and objectives; referring patients to specialists, and administering annual budgets.
Knowledge, skills, and abilities that can enhance success in this career include – knowledge of clinical operations and procedures, knowledge of modern principles and techniques of general medicine and public health, knowledge of community medical diagnostic and patient care services; understanding of relevant drugs and non-pharmaceutical patient care, and familiarity with current principles, methods and procedures. Medical Doctors with several years of experience holding the state licensure gains eligibility for this role.
Headline : As an Associate Medical Director, responsible for Ensuring that projects are technically accurate, audience-appropriate, and meet stated objectives, Researching and developing outlines and select references appropriate for a project.
Skills : Research, Math Tutor, Scientific Writing.
Description :
Responsible for providing medical oversight of clinical trials and pregnancy registries to ensure the safety of subjects and the scientific integrity of the studies.
Substantial experienced serving as regional lead medical monitor for a number of studies.
Ensured consistent medical monitoring and comprehensive safety surveillance across the program.
Provided medical oversight of multiple post-marketing pregnancy drug exposure registries in the role of sub-principal investigator.
Handled subject inclusion/exclusion queries and subject management issues requiring medical judgment.
Ensured appropriate content of safety narratives.
Wrote an analysis of similar events.
Experience
5-7 Years
Level
Executive
Education
MS
Associate Medical Director Resume
Objective : To establish a long-term career in a company where I may utilize my Associate Medical Director professional skills and knowledge to be an effective Associate Medical Director and inspiration to those around me.
Skills : MS Office, Medical Director, Multitasking.
Description :
Collaborated with New Product Development (NPD), Marketing, and Post Market Quality (PMQ) by acting as a team member to provide clinical input into product design improvements, product risk management, updates to labeling and/or promotional material which can help improve marketing strategy for device.
Reviewed all labeling and marketing/promotional material to ensure medical devices are marketed in accordance with claims made to the FDA relating to performance.
Reviewed customer complaints made by hospitals to ensure all patient safety issues are appropriately reviewed to determine Medical Device Reporting to the FDA/EU/ROW agencies.
Conducted Health Hazard Evaluations for all identified patient safety issues to determine whether or not a recall would be required.
Developed and maintained professional relationships with academic and community-based sites.
Researched to compile data to support the determination of severity and probability of harm for Post Launch Risk Assessments and Health Hazard Evaluations (HHE's).
Provided clinical recommendations to improve product so as to increase detectability of product failure at point of use so as to minimize patient impact.
Experience
2-5 Years
Level
Junior
Education
BS
Associate Medical Director Resume
Headline : Seeking an Associate Medical Director position with an outstanding career opportunity that will offer a rewarding work environment along with a winning team.
Directed oversight of clinical operations including inpatient and outpatient services and care management, case management, disease management, concurrent review, pre-certification, quality, ancillary service providers, and pharmacy with an average staff of 25-30 and an operating budget of over $2 million.
Increased enrollment in case management and disease management programs by over 150% by setting clear performance expectations in regards to caseloads, timely enrollments, interventions, care plans, provider involvement, outcomes, productivity, etc.
Built infrastructure through the establishment of well-defined processes/guidelines, removal of barriers that prevented early 3 Montgomery MD Vergena Montgomery, Clark, MD, MBA/HSA Resume identification, timely enrollment, CM initiation, established standards timeframes for completion of these activities and appropriate program discharge and finally implementation of a Case Management Audit program for monitoring and evaluation.
Decreased pmpm cost by 50% for case management, 51% for CHF, and 30% for Rare Diseases by decreasing acute admissions, acute bed days, and ER visits, and increasing patient compliance.
Averaged 40% enrollment in the first trimester as a result of the Pre-natal case management program.
Successfully transitioned the physical location and operations of the referral unit from the service center in Jacksonville, Florida to the local Orlando market in less than 60 days.
Worked with Manager, Quality Systems to provide medical perspective/background, if needed, to respond to inquiries by international authorities.
Experience
5-7 Years
Level
Executive
Education
Doctorate Of Medicine
Associate Medical Director Resume
Headline : As an Associate Medical Director, responsible for Proactively beginning to monitor and identify relevant literature and provide a point of view to internal team and clients as needed, Learning to review content not just for accuracy but to determine if it is in line with product strategy.
Skills : Analytics, Clinical Terminology, Leadership, Team Creation, Mentoring, Patient Engagement, Population Health, Epic Systems Software, Particularly Ambulatory, And Cogito.
Description :
Ability to communicate effectively with physicians, pharmacists, and other health care professionals on medical education, clinical practice, presentation skills, and sharing information with for health information technology.
Skilled at presenting complex scientific data in a clear and concise manner, ability to analyze and solve complex scientific data into marketing and educational concepts.
Experienced in obtaining and leveraging information in the public domain to support proprietary marketing, business case creation, and creation of CME materials and improved IT workflow issues.
Able to work independently and to liaise with pharmaceutical executives and opinion-leading physicians, scientists, and researchers for improved publications, symposiums, computerized case sharing.
Created promotional PowerPoint slide decks, interactive CD-ROMs, online case studies, and newsletters on multiple topics in anticoagulation, diabetes, cardiology, infectious disease, neurology, oncology, pain management, psychiatry, pulmonary, multiple sclerosis, rheumatology, and pharmacology.
Designed and produced content for a series of live promotional programs, often presented materials, optimize workflow issues onsite.
Extensived participation in the content review process at major pharmaceutical companies, key opinion leaders in the medical community, faculty meetings, research seminars, clinical implementation for new medications, and insurance issues.
Experience
5-7 Years
Level
Executive
Education
BS In Pharmacy
Associate Medical Director Resume
Headline : Highly qualified Associate Medical Director with experience in the industry. Enjoy creative problem solving and getting exposure on multiple projects, and would excel in the collaborative environment on which your company prides itself.
Skills : Microsoft, Meditech, Siebel.
Description :
Provided cross coverage for marketed oncology, metabolic, anti-infective, and cardiovascular products.
Provided team leadership required for successful pharmacovigilance-related negotiations with licensing partners including the development, execution, and maintenance of the Safety Data Exchange Agreements (SDEA) and associated safety databases.
Led several Medical Surveillance Teams (multidisciplinary teams) responsible for the creation and implementation of medical surveillance, proactive safety signal detection strategies.
Led team to develop PV plans and Risk management plans (EU and US) at various stages of product development.
Prepared timely responses to regulatory agency queries, perform aggregate analyses of adverse event cases (preparation of PSUR's, PADER's, and ad hoc Expert Reports, Safety Summaries, and preparation of Risk Management Plans) and when appropriate, recommended labeling (CPLP, USPI, and SmPC) changes based on those analyses.
Provided contract medical communications services including medical writing and editing for newsletters, posters, monographs, supplements, slide kits, web pages, on-line case studies, and other promotional materials.
Worked with Manager, Quality Systems, and Manager Complaints to provide medical perspective or differences in standard of care which can affect complaints received from different geographies.
Experience
5-7 Years
Level
Executive
Education
BS
Associate Medical Director Resume
Headline : As an Associate Medical Director, responsible for Participating in proprietary workshops. Client Relationships Develop a relationship with client medical if/when appropriate, Participating in medically-relevant client interactions.
Skills : Communication Skills, Medical Skills, Planning.
Description :
Directed freelance medical writers in the completion of primary and review manuscripts, abstracts, slide decks, posters, and literature searches that fulfill author and client expectations.
Supported new business development and write needs assessments for compliant publication plans and continuing medical education initiatives.
Coordinated publication plans for armodafinil (Cephalon), mipomersen (Genzyme), and Aggrenox (Boehringer Ingelheim).
Participated in new business development for trisenox (Cephalon Oncology), otelixizumab (Tolex), and mipomersen (Genzyme).
Rewritten incomplete manuscripts for the Aggrenox publication plan (Boehringer Ingelheim).
Created slide kits and write executive summaries for advisory boards about mipomersen (Genzyme) and trisenox (Cephalon Oncology).
Wrote educational needs assessment for CME activities about mipomersen (Genzyme).
Experience
5-7 Years
Level
Executive
Education
Ph.D. In Immunology/Microbiology
Associate Medical Director Resume
Summary : A seasoned physician executive with over 20 years of clinical practice, ambulatory health care administration, quality, and process improvement experience. Had increasing levels of expertise and governance over a variety of Health Care Information Technology. Became board certified in Clinical Informatics.
Skills : Consulting, Biomedical, Communication.
Description :
Provided medical expertise on marketed HIV drugs to the organization (including copy and publication review), physicians, the HIV infected community, and the federal government.
Directed, provided medical expertise and budget oversight for phase 3b/4 clinical trials.
Representative to activist groups in New York, Paris, and Brussels Representative to Pfizer Advocates, a lobbying group in Washington, D.C.
Established and maintained an effective working relationship with Pfizer Pharmaceutical Group Regulatory and Commercial Units and with Pfizer Global Research and Development Clinical Development Unit.
Provided medical and scientific input to Strategic Planning and Business Development for approved drugs, virology drugs in development, and to R&D clinical development teams for virology drugs in development Consultant to the PGRD Clinical PK Group for PGRD phase 1 studies.
Provided medical and scientific input to Regulatory group with respect to toxicology issues, and FDA interactions and submissions Responsible physician for delavirdine sNDA, Investigator Brochure, PSUR, NDA and IND annual reports Representative to FDA, EMEA meetings.
Directed patient care responsibilities including management of acute withdrawal, management of acute and chronic medical problems, patient education, and coordination of aftercare.
Experience
10+ Years
Level
Senior
Education
MS
Associate Medical Director Resume
Objective : Highly qualified Associate Medical Director with experience in the industry. Enjoy creative problem solving and getting exposure on multiple projects, and I would excel in the collaborative environment on which your company prides itself.
Actively worked with utilization review to advocate for insurance coverage.
Performed medical review of Serious Adverse Events (SAEs) to identify appropriate follow-up requests and to assess expectedness, seriousness, and causality.
Depended on account size and needs, may serve as the lead clinical team member or work in collaboration with other clinical team members, to drive the account or projects within the account.
Actively participated with the team on strategic planning, ranging from crafting a brands strategic imperatives and scientific pillars to engaging with the internal or external team to develop a tactical plan that will effectively execute on a brands aligned upon strategy.
Worked with the account team and other members of the clinical team to develop a strong client partnership and build the clients confidence in Symbiotixs ability to activate their science in a meaningful and effective way.
Effectively led the clinical portions of client meetings, providing strategic guidance and direction, and demonstrating full command of the therapeutic area.
Confidently engaged with key opinion leaders and other client groups of interest, as needed.
Experience
2-5 Years
Level
Junior
Education
MS
Associate Medical Director Resume
Objective : Associate Medical Director with 3+ years of experience in Contributing to brand planning process with supervision. Responsible for Helping to develop a communication platform (or scientific platform for medical education) that will serve as an internal content roadmap and foundation for communications.
Piloted new projects involving the medical community in alliance with global functions.
Supported regional Marketing by working closely with country scientific affairs managers on the development of medical communication, advises primary marketing personnel regarding features, benefits, and competitive advantages.
Participated in local, state, national, and international medical/industry governmental meetings, providing strategic guidance to the Division through participation in these key associations to influence policy and regulations regarding medical devices.
Built strong relationships and ties with outside stakeholders, including with key opinion leaders and patient communities, as needed.
Exhibited a professional image and demeanor, demonstrating adaptability and a dedication to exceptional client service, assisting with the resolution of concerns related to assigned areas.
Partnered with creative services to develop highly visual and engaging materials that maintain a high level of scientific accuracy and achieve our clients strategic objectives.
Participated in business development engagements related to areas of therapeutic expertise, providing strategic and clinical insight, and participating in pitches.
Experience
2-5 Years
Level
Executive
Education
BA
Associate Medical Director Resume
Headline : Seeking an Associate Medical Director position, responsible for leading and executing the development of content including data analysis for a wide range of complex projects, with minimal review/direction Independently and accurately incorporate strategic concepts into projects as well as guide others to do so.
Skills : Planning, Supervising, Leadership.
Description :
Provided strategic input for the R&D pipeline to support existing and future products.
Ensured medical excellence in execution and oversight of development-stage studies.
Partnered with business development to develop and pursue sound opportunities for new products through a focus on in-licensing of new compounds and technologies in late-stage development.
Facilitated and merged strong science into commercially viable products utilizing aggressive timelines; integrate scientific rigor, medical need, and commercial value into compelling clinical plans culminating in successful registration and launch.
Built strong relationships and ties with outside stakeholders, including key opinion leaders and patient communities, as needed.
Supported the development of reliable and high-value publication strategies for new and existing products.
Led global & regional clinical and scientific advisory boards and liaised with global & regional key opinion leaders on generating ideas for future product/device development, expanded labeling of existing products/devices, and scientific communication of safety/efficacy of current products.
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