Pharmacovigilance manager Work, Jobs in Paddington, Gtl (with Salaries)

Senior Manager Medical Information
Vertex Pharmaceuticals —Paddington
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- In-person
Associate Pharmacovigilance Project Manager
PrimeVigilance —London
- Full-time
- Remote
- English
- Project management
- Mentoring
Quick apply
10d
Senior Manager, PV Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
9d
Business Development Manager - Pharmacovigilance
Novumgen —Welwyn Garden City
- Full-time
- Hybrid work
- CRM software
- Sales
- Business development
- Free parking
- Work from home
Quick apply
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Senior Manager, Medical Communications
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Project management
Quick apply
Pharmacy Business Manager
IQVIA —London
- Microsoft Powerpoint
- Sales
- Communication skills
- Annual leave
- Employee discount
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
Nephrology Medical Affairs Senior Director
Vertex Pharmaceuticals —Paddington
- Full-time
- Management
- Supervising experience
- Communication skills
9d
Medical Director
Ellipses Pharma —London
- Doctoral degree
- Supervising experience
- Travel
Manager, Commercial Quality
PrimeVigilance —London
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
Quick apply
2d
Manager, Labelling Strategy and Development
GlaxoSmithKline —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
2d
Research Manager - Quantitative Market Research
APLUSA —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- Marketing
- Annual leave
Quick apply
Medical Director, Oncology
Caidya —London
- Remote
- Patient monitoring
- English
- Microsoft Office
Executive Director, Worldwide Operations Office - Pharmacovigilance
Regeneron —Uxbridge
- Doctoral degree
- Master's degree
- Bachelor's degree
- Annual leave
Associate Director Global Patient Safety
Regeneron —Uxbridge
- Nursing
- Communication skills
- Annual leave
3d
Senior Manager, Aggregate Reporting Management
Regeneron —Uxbridge
- PMP
- Analysis skills
- Project management
- Annual leave
4d
Associate Country Clinical Quality Manager
Fortrea —Maidenhead
- Full-time
- Analysis skills
- Bachelor's degree
Senior Clinical Research Associate - UK&IRE - 0.5FTE
ProPharma Group —London
- Part-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
13h
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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pharmacovigilance manager jobs near paddington, gtl

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 paddington, gtl

Senior Manager Medical Information

Associate Pharmacovigilance Project Manager

Senior Manager, PV Operations

Business Development Manager - Pharmacovigilance

Clinical Trials Manager

Senior Manager, Medical Communications

Pharmacy Business Manager

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

Nephrology Medical Affairs Senior Director

Medical Director

Manager, Commercial Quality

Manager, Labelling Strategy and Development

Research Manager - Quantitative Market Research

Medical Director, Oncology

Executive Director, Worldwide Operations Office - Pharmacovigilance

Associate Director Global Patient Safety

Senior Manager, Aggregate Reporting Management

Associate Country Clinical Quality Manager

Senior Clinical Research Associate - UK&IRE - 0.5FTE

Managing Director, R&D Consulting

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