Medical Affairs

Medical Affairs

Product development never rests. With new sophisticated molecules, medical devices, and even gene therapies, there is a higher demand for clinical and drug information, creating new career opportunities for pharmacists in the growing area of medical affairs. To quote Albert Einstein, โ€œMake everything as simple as possible, but not simpler.โ€ Medical Affairs teams are the medical face of the company and their value lies their ability to disseminate information as accurately and precisely as possible without changing its meaning.

The medical affairs sector as a whole is growing in popularity, according toKyle Kennedy, vice president of customer strategy with the Medical Affairs Company (TMAC), โ€œI have always said a position in medical affairs is the best job in the pharmaceutical sector. You learn so many skills that prepare you to be successful in other positions in the industry. In medical affairs, you have opportunities to work in or with clinical trial activities, medical information, competitive intelligence, pharmacovigilance, medical writing, health outcomes, scientific platform communications, and key opinion leader development, and you may even be able to move over to the commercial side of industry, such as marketing.โ€

The Medical Affairs Professional Society(MAPS) is the premier non-profit global society of medical affairs professionals across a spectrum of fields, experience, and locales. The European branch of MAPS is headed up byEMEA President, Danie du PlessisMD, MBA.MAPS Vaulthosts an array of valuable resources addressing critical issues for medical affairs professionals, from current trends in medical affairs to changes in government laws that may impact our profession.

The future in terms of job growth looks positive for the sector,William Soliman, PhD, chair of the Accreditation Council for Medical Affairs says, โ€œMedical affairs has grown over 300% globally in the last decade and it will continue to do so, there are many more career opportunities than ever before.โ€

EPM Scientific is a global specialist recruitment company working exclusively in the Life Sciences industry. Our expert consultants place the best talent in the medical affairs industry in Germany and across Europe.

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Benefits of working with us

Experience

We have over a decadeโ€™s worth of experience as a leading talent partner in Life Sciences & Pharma.

Network

A vast, global network of the best, in-demand professionals, working with the worldโ€™s largest Life Sciences institutions, to take drugs, devices and therapeutic applications through from conception to completion.

Knowledge

Our award-winning talent specialists offer bespoke, tailored guidance on the latest hiring trends and industry news to help you achieve your goals.

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Medical Affairs Jobs

Senior Medical Director, Clinical Devlopment & Medical Affairs

Title: Senior Medical Director of Clinical Development & Medical Affairs Location: New Jersey, USA OR Remote (Continental USA only) A mid-size pharmaceutical company is hiring a Senior Medical Director to join the Global Clinical Development and Medical Affairs team. As Senior Medical Director, you will have oversight of a multi-disciplinary team and will lead the strategic planning and execution of a Clinical Development program, as well as the development of Medical Affairs strategy and publications planning for global product launches. Responsibilities: Oversee clinical trial design and execution (especially Phase 3 and Phase 4 studies) Lead Advisory Board meetings and KOL/Expert panels Provide medical and scientific expertise to the development of product, R&D, and Clinical Development plans Identify prospective principal investigators and key opinion leaders Contribute to regulatory dossiers and NDA submissions, participate in interactions/meetings with FDA, EMA, and other regulatory agencies Program management including people leadership, budget management, risk and contingency planning, etc. Contribute to publication planning; author publications as needed or applicable Skills & Qualifications: MD (or equivalent), PhD, or PharmD is required 5+ years of Clinical Development experience is required Expertise in Hepatology, Nephrology, Pulmonology, or Critical Care is strongly preferred Direct Medical Affairs experience is strongly preferred Experience working with global regulatory bodies (FDA, EMA, etc.) is required Experience in a Medical Device company is strongly preferred Compensation & Benefits Base Salary: $240,000-$260,000 Annual Bonus: 25% Long-Term Incentive package comprised of company stock (estimated value $60,000) Option for 100% remote (open to candidates in the continental USA) Excellent medical, dental, vision, and life insurance Generous PTO and sick leave policy

US$240000 - US$260000 per annum + 25% annual bonus, 25% RSU-based LTI
Bridgewater
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Product Manager (f/m/d)

Product Manager (m/f/d) for Neurology Introduction: We are currently seeking an experienced Product Manager to join our client's dynamic pharmaceutical company in Germany. The successful candidate will play a pivotal role in developing, executing, and managing brand plans tailored specifically to the MS market segment. Key Responsibilities: * Develop strategic brand plans that include positioning strategies and communication tactics. * Ensure effective execution of marketing campaigns through collaboration with cross-functional teams * Analyze market trends & customer insights - make recommendations based upon observations * Lead product launches by providing direction throughout all phases of launch planning/execution process Qualifications: The ideal candidate must have the following qualifications/skills - * Relevant experience working as a product manager within Pharmaceuticals industry and with Multiple Sclerosis * Excellent knowledge of Neurology/CNS * Strong analytical skills- ability to interpret complex data sets effectively * Excellent project management capabilities - able manage multiple projects simultaneously while adhering strict deadlines * Exceptional stakeholder engagement abilities If you're looking for your next career move where you can apply your expertise in driving growth within this innovative organization then we invite you submit your application today!

Negotiable
Germany
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Medical Information Specialist

One of EPM Scientific's key clients are currently searching for a Medical Information Specialist to join their team on a contract basis. They are a consultancy who are partnering with a large pharmaceutical company, who specialise in rare diseases. Please see the below responsibilities of the role: - Intake and documentation of Medical Information enquiries in IRMSData - Literature search for substantiating a medical information response - Drafting a medical information response - Adverse event/Product quality complaint reporting as per client procedures - Affiliate reconciliation activities with the DS Hub/as appropriate as well as with the Local Product complaint responsible Contract Details: - 7-9 month contract - Remote - ASAP start - Requirement: Fluent in German - Requirement: Pharmacist background The ideal candidate will have one years experience in a Medical Information Specialist or Medical Information Manager role, however they are open to seeing a variation of experience. If interested, please click the relevant links to apply! Looking forward to hearing from you!

Negotiable
Deutschlandsberg
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Senior MSL - Respiratory, SW

Title: Senior Medical Science Liaison Territory: Southwestern US An evolving international research focused pharmaceutical company dedicated to the advancement and advocacy of products tailored for the hospital, related specialty, and rare disease sectors is seeking a highly motivated and well experienced Senior Medical Science Liaison (MSL) to support their growing respiratory pipeline. Position Summary The Senior MSL will be a field-based, external facing member of the Medical Affairs business unit. Primary duties will be forging partnerships with key opinion leaders (KOLs) through the exchange of scientific data and other pertinent medical or scientific insights with external stakeholders (such as healthcare professionals, researchers, leadership from professional organizations, patient advocacy groups, and decision-makers involved in formulary management) within the designated Therapeutic Areas (TAs). This team will specifically be focusing on Respiratory conditions (COPD/Asthma) within the specified geographic region. Key Responsibilities 1. KOL Engagement: Develop and maintain professional relationships with KOLs and HCPs aligned with individual territory plans. Demonstrate advanced knowledge of products, competitor landscape, and therapeutic area. Communicate complex scientific information to KOLs/HCPs in a compliant, fair-balanced, and non-misleading manner. 2. Research Support: Recognize and seize opportunities to offer medical assistance, including scientific education, to healthcare professionals (HCPs) within prominent institutions. Cultivate professional connections within pivotal institutions across designated geographic areas. Identify prospects for promoting cross-functional collaboration in response to customer requirements. 3. Partnership Building: Identify and cultivate partnership opportunities between KOLs/HCPs and US Medical. Collaborate with cross-functional teams to enhance medical strategy. 4. Medical Conferences: Participate in executing medical strategy at conferences (e.g., staff medical booths, attend sessions, interact with KOLs/HCPs). Qualifications Advanced Degree: PharmD, MD, PhD, or equivalent. Experience: Previous MSL experience is required (minimum 2+ years) - working within respiratory therapies for COPD/Asthma is also a must have. Communication Skills: Excellent verbal and written communication skills. Travel: Ability to travel within the assigned territory as needed. Benefits Comprehensive benefits package, including health insurance, retirement plans, and professional development opportunities.

Negotiable
England
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