Medical Affairs Professional Job at CK Group (Basingstoke)

Associate Medical Director, US Medical Affairs

The Associate Medical Director will be responsible for contributing to and parti...

Location

United States , Morristown

Salary:

180000.00 - 210000.00 USD / Year

Alfasigma

Expiration Date

Until further notice

Requirements

MD/PhD/PharmD (or equivalent) with a minimum of 5 years of professional/clinical experience
At least 3 years of biopharmaceutical industry experience in Medical Affairs and/or Clinical Research is required
Experience working with professional societies and quality organizations preferred
Prior experience in Hepatology, Gastroenterology, or Immunology preferred
Ability to travel up to 20% required (mostly to congresses/ad boards), which may include overnight and/or weekend travel
Strong understanding of Medical Affairs functions, processes, and strategic execution
Track record of being held accountable for key individual deliverables with successful results required
Strong verbal and written communication skills are essential, including strong presentation skills
Excellent organization and multi-tasking skills
Strong interpersonal skills and problem-solving capabilities

Job Responsibility

Participate in the development of a cross-functionally aligned set of medical strategies for the US market needs, focused on commercialized as well as late-stage development indications/assets
Develop the strategy for professional medical association engagement in the US in conjunction with other US stakeholders as part of the broader professional society strategy
Support medical affairs data generation and dissemination working group(s) and collaborate with the Scientific Communications team to develop and execute aligned strategies/tactics for maximizing our scientific communication efforts
Support field medical activities and help to assess and address internal/external medical education needs in collaboration with the Field Medical and Scientific Communications teams
Perform scientific and clinical training for internal staff, including Commercial/Sales, on Alfasigma products and respective disease-related aspects
Lead and execute scientific advisory boards to generate strategic insights that inform medical affairs plans
Participate in or perform review of promotional and medical/scientific materials as the Medical Reviewer, following standard operating practices (SOPs) and in collaboration with Regulatory, Legal, and Commercial counterparts
Maintain strong relationships with the external thought leader and influencer communities
Contribute to, and support execution of the lifecycle management activities for Alfasigma’s commercialized indications/assets
Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team

What we offer

401(k) plan with company match
Rewards and recognition program
Health care benefits (medical, prescription drugs, dental, and vision insurance)
Short and long-term disability coverage provided
Plan coverage for domestic partners
Paid parental leave benefits and adoption assistance
Tuition reimbursement assistance
A generous Paid Time Off program that includes 20 vacation days, 11 holidays, 4 personal days, and 2 volunteer days per calendar year
Numerous well-being and work/life programs

Fulltime

Associate Medical Director, Medical & Scientific Affairs

At KARL STORZ, we are dedicated to improving patient outcomes through cutting-ed...

Location

United States , El Segundo

Salary:

229400.00 - 310200.00 USD / Year

KARL STORZ

Expiration Date

Until further notice

Requirements

MD or DO degree required
8+ years of surgical experience, including residency training (general surgery or closely related specialty preferred)
Strong foundation in medical device technology, clinical evaluation, and patient safety principles
Demonstrated ability to communicate complex scientific concepts to diverse internal and external audiences
Excellent leadership, collaboration, and organizational skills
able to thrive in dynamic, cross-functional settings

Job Responsibility

Serve as a clinical and scientific expert in general surgery, video and imaging platforms, and operating room integration products
Partner cross-functionally with R&D, Regulatory Affairs, Quality, Legal, and Commercial teams to ensure clinical accuracy and sound medical decision-making throughout the product lifecycle
Lead and support medical safety initiatives, including post-market surveillance, product recalls, and risk assessments to safeguard patient care
Engage with Key Opinion Leaders (KOLs), facilitate advisory boards, and lead scientific and educational programs to advance product knowledge and adoption
Collaborate with Clinical Affairs to assess and communicate clinical evidence, literature, and research insights that guide strategic decisions
Provide medical input for product development, regulatory submissions, and educational content for healthcare professionals
Represent KARL STORZ in external scientific forums and peer-to-peer clinical discussions while maintaining the highest standards of compliance and professionalism

What we offer

Medical / Dental / Vision including a state-of-the-art wellness program and pet insurance, too
3 weeks vacation, 11 holidays plus paid sick time
Up to 8 weeks of 100% paid company parental leave
includes maternal/ paternal leave, adoption, and fostering of a child
401(k) retirement savings plan providing a match of 60% of the employee’s first 6% contribution (up to IRS limits)
Section 125 Flexible Spending Accounts
Life, STD, LTD & LTC Insurance
We prepay your tuition up to $5,250 per year! - Tuition pre-imbursement
Fitness reimbursement of up to $200 annually

Fulltime

Medical Affairs Manager

Where scientific insight meets meaningful impact in patient care. Proclinical is...

Location

Belgium , Mechelen

Salary:

100000.00 - 120000.00 EUR / Year

Proclinical

Expiration Date

Until further notice

Requirements

A scientific or medical degree (e.g., physician, pharmacist, MSc in Biomedical Sciences, or similar).
Fluency in Dutch.
Experience in the pharmaceutical or biotech industry, ideally in Medical Affairs, clinical specialty products, or a related scientific role.
Proven ability to engage with external experts and key opinion leaders (KOLs) while adhering to compliance standards.
Exposure to nephrology, cardiorenal, cardiovascular, metabolic, rare diseases, or adjacent specialty medicine.
Strong communication, organizational, and independent working skills.

Job Responsibility

Develop and implement Medical Affairs strategies and tactical plans within the therapy area.
Build and maintain long-term relationships with external experts, healthcare professionals, and patient organizations.
Lead scientific exchanges, advisory boards, and medical education initiatives.
Support investigator-initiated and collaborative study discussions, including site feasibility assessments.
Provide scientific input into cross-functional plans, materials, reimbursement dossiers, and governance processes.
Stay updated on therapy area knowledge, including rare disease nephrology, cardiorenal medicine, and the competitive landscape.

Fulltime

Medical Affairs Manager – Women’s Health

Lead and strengthen Medical Affairs in Mexico by shaping and executing a forward...

Location

Mexico , Mexico City

Salary:

Not provided

Theramex

Expiration Date

Until further notice

Requirements

Medical degree, preferably with postgraduate qualifications in a relevant therapeutic area
Proven experience in Medical Affairs within the pharmaceutical industry, demonstrating ability to deliver strategic and operational impact
Minimum of 3 years working as a Medical Affairs Manager or in a comparable role
Fluency in Spanish and English (written and spoken)
Experience with Women’s Health products is considered a strong advantage
Knowledge of Mexican health regulations, including COFEPRIS standards and compliance requirements
Excellent interpersonal, communication, and scientific writing abilities
A self-driven, proactive professional with the capacity to manage multiple tasks of varying complexity and navigate a fast paced environment
Willingness to travel up to 30% of the working time

Job Responsibility

Maintain up to date clinical and scientific expertise in relevant therapeutic areas, providing strategic and operational insights to inform brand planning and decision making
Continuously review scientific literature and participate in key scientific events—such as congresses, symposia, and expert meetings—to ensure alignment with the latest medical developments
Provide timely, accurate, and fully compliant medical review and approval of promotional and non promotional materials, supporting business objectives while upholding the highest ethical standards
Partner closely with the Marketing and cross functional teams to develop and execute brand plans and deliverables for the Women’s Health portfolio
Collaborate with Marketing to plan and implement scientific meetings, educational programs, advisory boards, and symposia
Support broader organizational needs, including Medical Information and Pharmacovigilance activities, by providing scientific expertise and guidance

What we offer

Private Health and dental Insurance for employee and family members
Company’s car
Ticket Meals
Hybrid Working
Engaging employee experience to come together as a community: in-office events, shared learning and much more

Fulltime

Medical Affairs Program Manager

This position is a member of the Clinical Science & Office of Medical Affairs te...

Location

United States , Minneapolis

Salary:

108191.00 - 162287.00 USD / Year

Coloplast

Expiration Date

Until further notice

Requirements

5+ years’ experience within clinical research and/or medical affairs activities, preferably with medical devices
Bachelor’s degree (health science or biotech area)
Knowledge of and experience with ISO 14155, FDA, GCP, and MDR regulations
Ability to travel - 10%
Strong ability to review and interpret scientific data and research
Demonstrated ability to work across functions to prioritize and drive strategic objectives
Excellent oral and written communication skills
Excellent project management and organizational skills
An understanding of biostatistics and trial design
High degree of initiative and self-motivation with a strong sense of accountability

Job Responsibility

Serve as medical expert for relevant product(s) and associated clinical conditions
Oversee the medical affairs strategy development and implementation for designated area(s)
Support the required clinical input into documents including, but not limited to, instructions for use (IFUs), post-market clinical plans (PMCF), clinical evaluation reports (CERs), and other relevant documents
Support development and updates of Clinical Evaluation Reports (CERs) and associated documents as assigned (i.e. CER, PMCF, SSCP, PSUR, etc)
Develop and deliver medical device technical documents supporting product launch and sustaining activities
Leverage latest literature, regulations and guidance to build and execute on evidence strategies
Drive publications of data to ensure relevant content at medical congresses and at Coloplast events
Develop and deliver relevant medical device training documents (e.g. training decks, in-service scripts, eLearning tools, etc.) supporting product launch and sustaining activities
Supports with relevant medical writing expertise for evidence generation (e.g. white papers, clinical studies, publication plan, etc.)
Manage publication activities, as applicable

What we offer

Comprehensive medical, dental, and vision insurance plans
company sponsored wellness programs and mental health resources
paid leave of absence for qualifying events
generous paid parental leave for both birthing and non-birthing parents
competitive 401(k) plan with company match that vest immediately
financial planning services
corporate discount programs for goods and services
generous paid time off
flexible work hours
flexible work arrangement options

Fulltime

Senior Regional Medical Affairs Manager Center South -Lung Cancer (RMAM)

You will lead regional medical affairs in your area of Germany, building trusted...

Location

Germany , Munich

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Advanced degree in medicine, pharmacy, life sciences or related field (MD, PharmD, PhD or equivalent)
Minimum 3 years ideally experience in medical affairs, medical science liaison, clinical research in lung cancer
Strong clinical and scientific knowledge relevant to the therapy area
Excellent verbal and written communication skills in German and English
Willingness and ability to travel regularly within the assigned region
Solid understanding of regulatory, ethical and compliance requirements in the pharmaceutical environment.

Job Responsibility

Build and maintain scientific relationships with healthcare professionals and external clinical experts in the region
Deliver evidence-based medical education and scientific exchange in person and using digital channels for the area lung cancer
Respond to medical and scientific enquiries from healthcare professionals in a timely and compliant way
Support clinical research collaborations, including identifying study centres and enabling investigator-initiated research
Capture, synthesize and share local clinical insights to inform medical strategy and cross-functional planning
Plan and run regional medical activities such as advisory boards, symposia and educational meetings.

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes.

Fulltime

Senior Manager, Global Medical Affairs (Uterine Health)

We are seeking a highly motivated and experienced Senior Manager, Global Medical...

Location

United Kingdom , London

Salary:

Not provided

Theramex

Expiration Date

Until further notice

Requirements

Medical degree with GMC registration or equivalent international qualification or Master of Pharmacy with GPhC registration
Previous experience in Medical Affairs, Clinical Research, or Pharmacovigilance within the pharmaceutical industry
Very good understanding of Medical Affairs' role as scientific enabler and strategic partner in a pharmaceutical company
Strong knowledge and subject matter in women's health
Ability to cut through scientific complexity and to communicate precisely and clearly with different target audiences
Strong interpersonal and leadership skills and track record of expertise working in a cross-functional environment
Strong analytical and strategic thinking
Strong business acumen
Highest professional work ethics
Proven knowledge of the ABPI Code of Practice and codes of international associations of the pharmaceutical industry, with experience in reviewing and/or certifying materials.

Job Responsibility

Develop and implement medical plans aligned with business objectives and manage associated budgets
Provide expert medical input across the product lifecycle including evidence generation, evidence dissemination (e.g. health care professional education programs), and medical experts’ engagement programs (e.g. advisory boards)
Build and maintain relationships with international therapy area experts and medical-scientific professional societies
Act as a medical reviewer for promotional and non-promotional materials in line with the ABPI and international associations of the pharmaceutical industry codes as well as internal SOPs
Support regulatory and market access submissions with clinical content
Ensure compliance with all relevant regulations and contribute to continuous process improvement
Ensure operational excellence.

Fulltime

Senior Director, Global Medical Affairs – Front Line Care

Senior Director, Global Medical Affairs – Front Line Care (FLC) is the senior me...

Location

United States , Skaneateles Falls

Salary:

280000.00 - 385000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

8-10+ years of industry experience, including meaningful experience in MedTech
5+ years of strategic leadership/management experience, including people leadership in a matrixed environment
Demonstrated experience developing and implementing global evidence roadmaps
Leading/partnering on clinical evidence strategy, scientific communications, and cross-functional decision-making
Strong understanding of the U.S. and Global regulatory and healthcare environment including EuMDR and notified bodies requirements
Proven track record to operate with high integrity and in alignment with compliance standards
Demonstrate solid proficiency in study build, clinical trial methodology
Applicants must be authorized to work for any employer in the U.S.

Job Responsibility

Define and implement the FLC Global Medical Affairs strategic plan and critical evidence priorities
Provide senior medical leadership and decision support for business strategy, innovation, and new product development
Translate clinical, scientific, and customer insights into clear strategic recommendations and measurable execution plans
Develop global clinical evidence roadmap enabling execution of the global business priorities
Serve as a senior representative for FLC with KOLs, professional societies, advisory boards, and scientific conferences
Build strong, trusted partnerships across R&D, Regulatory Affairs (RA), Quality, Marketing, Reimbursement, Regions, Market Access, and Patient Safety
Partner with Global Patient Safety as a product/therapy to provide subject matter expert support
Provide expert medical/scientific leadership for due diligence on business development opportunities
Lead, coach, and develop a high-performing Medical Affairs team.

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

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