Pharmacovigilance manager Work, Jobs in Hemel Hempstead, Hrt (with Salaries)

Senior Manager Medical Information
Vertex Pharmaceuticals —Paddington
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- In-person
Senior Manager, Patient Safety Scientist
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Analysis skills
Regional Pharmacovigilance Officer
MSD —London
- Full-time
- Hybrid work
- Travel
4d
Associate Pharmacovigilance Project Manager (Europe)
PrimeVigilance —London
- Full-time
- Remote
- Project management
- Mentoring
- Leadership
Quick apply
Senior Manager, PV Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Senior Manager, PV Process Quality Lead
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Microsoft Office
- Bachelor's degree
- Travel
Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
- Communication skills
Senior Manager, Medical Communications
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Project management
Quick apply
Research Manager - Quantitative Market Research
APLUSA —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- Marketing
- Annual leave
Quick apply
Associate Country Clinical Quality Manager
Fortrea —Maidenhead
- Full-time
- Analysis skills
- Bachelor's degree
International Sales Manager
Datrax Services Pvt Ltd —London
- £3,000.00 - £3,500.22 a month
- Full-time
- Sales
- Marketing
- Master's degree
Quick apply
3d
12 month FTC- Spanish speaking Medical Information Specialist
ProPharma Group —London
- Full-time
- Hybrid work
- Spanish
- English
- In-person
11d
Director, Business Development - UK
RxLogix Corporation —London
- Full-time
- Remote
- Sales
- Customer service
- Presentation skills
Quick apply
Medical Director
Ellipses Pharma —London
- Doctoral degree
- Supervising experience
- Travel
Managing Director, R&D Consulting
Syneos Health Commercial Solutions —London
- Microsoft Powerpoint
- Microsoft Excel
- Master's degree
Managing Director, R&D Consulting
サイネオス・ヘルス —London
- Microsoft Powerpoint
- Microsoft Excel
- Master's degree

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Senior Manager Medical Information

Vertex Pharmaceuticals -
Paddington

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Job details

Full-time

Qualifications

Analysis skills
Bachelor's degree
Legal drafting
Epidemiology
Communication skills

Full job description

Job Description

General Summary:

The Senior Manager Medical Information drafts and maintains medical information content for use by the Medical Information Call Center (MIC) staff to respond to medical inquiries from healthcare professionals
and patients. The Senior Manager Medical Information reviews MIC case records for accuracy of response and appropriate case processing in compliance with applicable policies, SOPs and country specific
regulations and/or guidance.

Key Duties and Responsibilities:

Develops and maintains in-depth therapeutic knowledge of disease, epidemiology, product and competitor product information to facilitate the creation of medical content.
Drafts standard medical response letters and frequently asked questions (FAQs) for assigned product(s) and/or investigationals that are timely, non-misleading, accurate, and scientifically balanced for assigned Vertex marketed products and/or investigationals and relevant diseaserelated topics for use by MICs to respond to commonly received unsolicited medical inquiries.
Provides guidance to Medical Information Managers on the appropriate methods for drafting standard medical responses (letters and FAQs).
Works cross-functionally with other subject matter experts (SMEs) in Medical Affairs, Regulatory Affairs, Formulations and Pharmacovigilance to send response drafts (letters and FAQs) for review and approval to ensure drafts are accurate, compliant and appropriately address the topic of the inquiry. Creates standard language templates based upon SME review and approval.
Utilizes therapeutic knowledge and clinical expertise to independently draft timely, nonmisleading, accurate, and scientifically balanced custom responses to new and/or unusual unsolicited medical information inquiries concerning assigned product(s). Provides guidance to
Medical Information Managers on the appropriate methods for drafting custom medical responses.
Reviews medical information call center case records (medical inquiries, potential adverse events, and potential product complaints) to ensure quality and accuracy of response and appropriate case processing.
Drafts metric and insight reports for use by medical information upper management and strategic business partners.
Fact checks medical and marketing content, related to assigned product(s) and/or investigationals in the electronic review and approval system, for accuracy and appropriateness and relays all discrepancies to the appropriate subject matter expert or final approver.
Monitors the medical literature for additional sources of product information and content for use in the creation of medical information materials

Knowledge and Skills:

Excellent oral and written communication and literature searching skills to explain difficult information
Experience drafting medical information content with a high degree of accuracy and accountability
Sound knowledge of the stages of drug development and the available corporate and public resources used to construct a medical information response
Ability to work collaboratively in a dynamic, team-based matrix environment and to function independently as appropriate
Strong working knowledge of the rules and regulations governing the provision of Medical Information in Pharma
Analytical skills and an ability to synthesize data sets and study summaries into meaningful oral or written communication materials

Education and Experience:

Bachelor’s degree in a health-related science
Typically requires 6 years experience, with 2 years experience working in either Medical Information or Medical Affairs in a biotech/pharma or equivalent combination of education and experience.

Flex Designation:

Remote-Eligible

Flex Eligibility Status:

In this Remote-Eligible role, you can choose to be designated as:
1. Remote : work remotely five days per week and come into the office on occasion – you’re always welcome on-site; or select
2. Hybrid : work remotely up to two days per week; or select
3. On-Site : work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Remote

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [email protected]

Apply Now

Refine Your Search

pharmacovigilance manager jobs in hemel hempstead, hrt

Senior Manager Medical Information

Senior Manager, Patient Safety Scientist

Regional Pharmacovigilance Officer

Associate Pharmacovigilance Project Manager (Europe)

Senior Manager, PV Operations

Clinical Trials Manager

Senior Manager, PV Process Quality Lead

Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)

Senior Manager, Medical Communications

Research Manager - Quantitative Market Research

Associate Country Clinical Quality Manager

International Sales Manager

12 month FTC- Spanish speaking Medical Information Specialist

Director, Business Development - UK

Medical Director

Managing Director, R&D Consulting

Managing Director, R&D Consulting

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