Jobs

Medical Affairs Manager - Cardiovascular/Metabolism
CZE - Central Bohemian - Prague (Five)
·
On-site
·
Full-time
·
1w ago
Benefits & Perks
•Healthcare
•Pension
•Parental Leave
•Learning Budget
•Flexible Hours
•Gym
•Commuter Benefits
•Healthcare
•Parental Leave
•Learning
•Flexible Hours
•Gym
•Commuter
Required Skills
Biological Sciences
Business Strategies
Clinical Trial Planning
Cross-Functional Collaboration
English Language
Medical Affairs
Medical Knowledge
Medical Training
Pharmaceutical Medical Affairs
Job Description:
Medical Affairs Manager
- Cardiovascular/Metabolism
Overview:Under the supervision of the Medical Director, the Medical Affairs Manager (MAM) oversees medical activities for one or more therapeutic areas, collaborating with marketing, market access, policy teams.
Key Responsibilities:
-
Strategic Contribution: Optimize medical and clinical excellence throughout the product lifecycle to meet business objectives.
-
Medical Affairs Strategy: Develop and implement the Medical Affairs Plan (MAP) for assigned therapeutic areas, managing related budgets.
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Scientific Interactions: Establish and maintain high-level scientific relationships with healthcare professionals (HCPs), including scientific leaders and societies.
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Advisory Role: Provide medical and scientific input for business strategies, market access, and health economics.
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Expert Recognition: Serve as the company’s expert in the therapeutic area among HCPs and colleagues.
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Regulatory Engagement: Engage with regulatory and reimbursement authorities on scientific and medical matters.
Strategic Activities:
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Local Planning: Implement local Medical Affairs activities to enhance the company’s reputation and represent it in cross-functional teams.
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MAP Development: Create a MAP with strategies aligned to brand imperatives and local healthcare needs.
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Data Generation: Plan and execute local data generation programs, ensuring compliance with product strategies and securing necessary approvals.
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Publication Management: Implement publication policies and secure the production of review articles.
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Event Participation: Identify and engage in relevant meetings, congresses, and CME opportunities.
External Interactions:
-
Scientific Leadership: Maintain dialogue with scientific leaders and manage national/regional Advisory Boards.
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CME Contributions: Participate in sponsored meetings and CME events, including speaker engagements and presentations.
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Guideline Input: Provide input for formulary and clinical guideline development.
Internal Interactions:
-
Cross-Functional Partnership: Be a valuable partner in cross-functional teams. Act as the medical and scientific expert for therapeutic areas, collaborating with Market Access, Marketing, Policy, Regulatory, and Clinical Operations.
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Promotional Accuracy: Ensure the scientific accuracy of promotional materials through the review process.
Skills, Knowledge & Competencies:
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Proficient understanding of drug development, relevant diseases, and local medical practices.
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Strong knowledge of therapeutic areas and applicable regulations.
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Effective collaboration in a matrix organization.
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Excellent interpersonal and presentation skills.
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Strong ethical standards and leadership behaviors.
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Open-mindedness, willingness to learn, and a mindset for sharing ideas.
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Strategic thinking.
-
Proficiency in English and Czech.
Education & Experience:
- Medical Degree (preferred) or PharmaD or PhD in life sciences.
What we offer:
-
Exciting work in a great team, global projects, international environment
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Opportunity to learn and grow professionally within the company globally
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Pension and health insurance contributions
-
Internal reward system plus referral program
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5 weeks annual leave, 5 sick days, 15 days of certified sick leave paid above statutory requirements annually, 40 paid hours annually for volunteering activities, 12 weeks of parental contribution
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Cafeteria for tax free benefits according to your choice (meal vouchers, Lítačka, sport, culture, health, travel, etc.), Multisport Card
-
Vodafone, Raiffeisen Bank, Foodora discount programs
-
Up-to-date equipment
-
Competitive salary, incentive pay, and many more
Ready to take up the challenge? Apply now!Know anybody who might be interested? Refer this job!
Required Skills:
Biological Sciences, Business Strategies, Clinical Trial Planning, Cross-Functional Collaboration, English Language, Medical Affairs, Medical Knowledge, Medical Training, Pharmaceutical Medical Affairs
Preferred Skills:
Current Employees apply HERE:
Current Contingent Workers apply HERE:
Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Hybrid
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
02/25/2026
A job posting is effective until 11: 59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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About Merck

Merck
PublicMultinational pharmaceutical company.
10,001+
Employees
Rahway
Headquarters
Reviews
3.6
19 reviews
Work Life Balance
3.8
Compensation
3.2
Culture
3.0
Career
2.8
Management
2.5
60%
Recommend to a Friend
Pros
Large company with networking opportunities
Good work-life balance
Decent benefits and salary
Cons
Limited upward and lateral mobility
Slow promotion timeline
Favoritism in advancement
Salary Ranges
2,500 data points
Director
Director · Associate Director, D&A Strategy
1 reports
$176,890
total / year
Base
$153,800
Stock
-
Bonus
-
$176,890
$176,890
Interview Experience
20 interviews
Difficulty
2.9
/ 5
Duration
14-28 weeks
Offer Rate
25%
Experience
Positive 10%
Neutral 50%
Negative 40%
Interview Process
1
Application Review
2
Recruiter Screen
3
Hiring Manager Interview
4
Panel Interview
5
Final Decision
Common Questions
Technical Knowledge
Behavioral/STAR
Past Experience
Culture Fit
Case Study
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