Senior Manager/ Manager – Medical Information Job at Theramex (London)

Senior Medical Information Manager

SRG are partnered with a leading Global Pharmaceutical Company who have an oppor...

Location

Ireland , Dublin

Salary:

33.00 - 38.00 GBP / Hour

SRG

Expiration Date

Until further notice

Requirements

Life sciences degree and/or postgraduate qualification
Significant experience within Medical Information (ideally including above country level experience)
Strong knowledge and application of good practices in medical enquiry management and writing for medical information
Experience with reviewing medical/clinical content and providing constructive feedback
Strong cross-functional skills and proven experience in collaboration with other departments/groups

Job Responsibility

Handle Medical Information (MI) enquiries in an efficient and appropriate manner
Collaborate with the MI function in the affiliate countries to ensure consistency and alignment in communication
Provide product related, clinical guidance to sales & marketing teams
Supporting Medical Information activities at congresses
Developing content for digital platforms

Fulltime

Senior Medical Marketing Manager

As the company's medical science expert for designated therapeutic areas, establ...

Location

China , Beijing

Salary:

Not provided

Coloplast

Expiration Date

Until further notice

Requirements

Master's or doctoral degree in clinical medicine, pharmacy, pharmacology, or related life sciences (MD, PhD, PharmD preferred)
At least 5 years Medical advisor experience in MNC pharmaceutical or medical device companies
Deep understanding of medical and clinical benefits of strategic products with business acumen
Strong process and numerical skills with an analytical approach to marketing and ability to identify and report on trends and insights
Highly self-motivated and willing to win attitude
Multi tasks & priority setting skill
Logic thinker & good analytic skill
Good English skill (including writing, reading and oral)
Team spirit
Good presentation skills (Including being well versed in MS Office applications)

Job Responsibility

Annual medical marketing and medical education plan development which is aligned with ABP & medical marketing strategies and plan
Provide medical and scientific input to promote a higher standard of ostomy care, thereby strengthening Coloplast leading position today and in the future
Plan post-market clinical studies to address evidence gaps and support product differentiation advantages. Conduct in-depth medical interpretation of existing clinical data to generate medical insights
Develop strong partnerships with national KOLs and gather KOL insights to drive stronger strategic medical perception and product adoption and usage with cutting edge medical evidence and educational material/tools
Organize and participate in AB meetings to conduct in-depth discussions on academic promotion strategies
Respond promptly, accurately, and in compliance to complex medical inquiries raised by external experts and internal colleagues
Responsible for developing and managing medical information materials, including medical reference manuals, product evidence summaries, and compilations of the latest clinical data
Conduct medical review of all external materials (including PPTs, DA, meeting materials, etc.) to ensure scientific accuracy, balanced content, and compliance with regulations and company policies
Provide in-depth content and training support to the sales, marketing and market access teams on topics such as disease knowledge, product functions, clinical data and information on competing products
Provide comprehensive medical support and preparatory work for new product launches and approvals of new indications

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

Medical Science Liaison or Senior Medical Science Liaison

The Skeletal Conditions (SC) Medical Science Liaison (MSL) / Senior MSL is a reg...

Location

United States

Salary:

178200.00 - 267400.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

BA/BS in life or health sciences
Advanced degree (MS, doctoral level) preferred
3 or more years of relevant experience in clinical and 1 or more year as an MSL preferred
Experience in rare genetic diseases, ACH and/or Skeletal Conditions therapy preferred
Experience in product launch, development, and execution preferred
Knowledge of regulations impacting Medical Affairs and field activities in the pharmaceutical industry
Excellent oral and written communication, organization, and people skills
Proven record as a team player
Project management understanding and experience
Ability to effectively work in a virtual environment and knowledge of virtual and collaborative systems

Job Responsibility

Execute SC medical MSL plan and tactics within assigned territory to meet scientific objectives and company-defined goals for products both marketed and in development
Development and periodic refinement of an approved MSL Territory Plan
Provide education relative to disease state and BioMarin products across product lifecycle to health care providers among specialties including Genetics, Pediatric Endocrinology, Pediatric Orthopedics, and other relevant specialties
Serve as a medical/scientific resource through answering unsolicited medical questions and addressing other related medical information queries
Engage in scientific exchange and provide feedback on emerging clinical/competitive trends
Identify, document, discuss and communicate insights to internal stakeholders
Maintain clinical and technical expertise in relevant therapeutic area
Partner with medical and research groups and compliantly collaborate with commercial team
Provide support to BioMarin clinical trials including but not limited to the following: site identification and evaluation
recruitment

What we offer

company-sponsored medical, dental, vision, and life insurance plans
discretionary annual bonus
discretionary stock-based long-term incentives
paid time off

Fulltime

Senior Medical Advisor – Rare Disease & Inflammatory Disease

In this senior role, you will provide medical leadership across Amgen's rare dis...

Location

United Kingdom , Cambridge

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Degree educated
Medical affairs experience, gained within pharmaceutical or biotechnology company
Previous people management and/or leadership experience leading teams, projects, programmes, or resources is desirable but not essential
Proven experience as a final ABPI signatory
Demonstrated ability to work independently while building strong cross-functional partnerships, leveraging strategic thinking, commercial acumen, agility, and effective communication to adapt quickly and deliver business objectives in a dynamic environment
Product/therapeutic area knowledge within rare diseases and/or inflammation experience is preferred, but not mandatory

Job Responsibility

Co-lead cross-functional brand strategy for designated products across the rare disease and inflammatory disease portfolio
Provide medical leadership to ensure global and regional strategy is translated effectively into local priorities and plans
Engage external experts, professional organisations, and other key stakeholders to inform strategy and strengthen scientific partnership
Partner with marketing, value and access, and other internal stakeholders to support lifecycle planning and patient access initiatives
Contribute to UK and Ireland affiliate strategy and tactical planning in close collaboration with regional and global colleagues
Support evidence generation planning, including collaboration on company-sponsored studies and review of investigator-sponsored study proposals
Work with clinical operations to identify appropriate sites and investigators for future company-sponsored research
Lead and develop assigned team members through effective line management, including coaching, performance development, capability building, and oversight of resource planning
Deliver therapy area and product-specific medical training to internal stakeholders as required
Provide medical review and approval support for promotional and non-promotional materials in line with applicable standards and governance

What we offer

Broad opportunities to develop your career and grow across a global organisation
An inclusive culture where colleagues are encouraged to contribute ideas, collaborate openly, and make an impact
A competitive total rewards package covering health, financial wellbeing, work-life balance, and career support
Flexibility for home working in line with business needs

Fulltime

Senior Manager Regulatory Affairs CZ&SK

Senior Manager Regulatory Affairs CZ&SK. Czech Republic - Prague. SALARY RANGE: ...

Location

Czech Republic , Prague

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of directly related experience OR Master’s degree and 6 years of directly related experience OR Bachelor’s degree and 8 years of directly related experience
Degree and in-depth regulatory experience and/or related to the affiliate
Depth knowledge of affiliate legislation and regulations relating to medicinal products
English and Czech and/or Slovak language working proficiency
Good negotiation and Influencing skills
Ability to anticipate and prevent potential issues
Ability to resolve conflicts and develop a course of action leading to a beneficial outcome
Cultural awareness and sensitivity to achieve results across both regional, affiliate and international borders
Ability to manage multiple activities and set priorities
Ability to lead teams and develop effective teams

Job Responsibility

Provides affiliate regulatory expertise and execution for the development, registration, and lifecycle management of all Amgen molecules
Oversee the affiliate and manage a regulatory team to ensure delivery of assigned local and ELMAC Regulatory initiatives
First point of contact for interactions with local regulatory agency(ies)
Ensure that the local Regulatory staff delivers assigned local and ELMAC Regulatory initiatives across the affiliates
Represent Regulatory on the affiliate leadership team
Provide local regulatory input to support development and execution of assigned Regulatory Affairs initiatives and effective interactions with key regulatory agency(ies)
Supervise and oversight for one or more regulatory staff
Manage and liaising with distributors (if applicable)
Translates assigned global, regional and ELMAC Regulatory initiatives into local regulatory objectives where applicable
Acts as senior point of contact for local regulatory advice on commercial and medical activities within the affiliate

Fulltime

Senior Manager, Market Intelligence & Customer Insights

Baxter’s Advanced Surgery business is one of the company’s most strategically im...

Location

United States , Deerfield

Salary:

152000.00 - 209000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Experience analyzing healthcare or medical device datasets such as Premier, SG2, DRG, IQVIA, or similar claims and utilization sources
Strong capability in Excel based modeling, forecasting, and market sizing
Working experience with SAS, R, or SPSS
SQL or Python
Familiarity with medical coding, procedure based analytics, and claims or charge level data
A demonstrated ability to translate complex analyses into clear, strategic insights for executive audiences
Strong communication and presentation skills, with the ability to influence across functions and levels
A proactive, intellectually curious mindset and comfort working independently on highly visible, recurring deliverables
A collaborative, low ego approach and the ability to thrive in a fast paced, cross functional environment
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time

Job Responsibility

Lead global market intelligence and competitive insights across hemostats, sealants, adhesion prevention, and adjacent surgical categories
Own annual global market sizing and forecasting, partnering with regional teams and aligning assumptions with Finance
Deliver biannual market share and competitive landscape analyses to inform portfolio and long‑range planning
Manage quarterly U.S. market size and growth reporting by integrating SG2, IQVIA, DRG, Premier, and internal performance data
Conduct hands‑on Premier analytics to understand procedural trends, product utilization, and specialty‑level dynamics
Translate complex data into clear, executive‑ready insights and strategic recommendations for senior leadership
Support M&A, licensing, and partnership evaluations through market sizing, competitive assessments, and scenario modeling
Build compelling narratives and present findings to cross‑functional stakeholders across Marketing, R&D, Medical, Regulatory, Finance, and Commercial

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), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
Commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

Global Regulatory Writing – Senior Manager

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of directly related experience OR Master’s degree and 6 years of directly related experience OR Bachelor’s degree and 8 years of directly related experience OR Associate’s degree and 10 years of directly related experience OR High school diploma / GED and 12 years of directly related experience
Ability to independently analyze scientific data and interpret its significance in practical applications
Excellent written/oral communication skills and attention to detail
Highly skilled in word processing and other Microsoft Office programs
Expertise in scientific/technical writing and editing, and of overall clinical development process for new compounds
Must demonstrate strong leadership skills in a team environment which requires negotiation, persuasion, collaboration, and analytical judgment
Ability to understand, follow, and develop complex standard operating procedures (SOP’s), guidance documents, and work instructions
Excellent time and project management skills
Self-starter with a drive and perseverance to achieve results and motivate others

Job Responsibility

Author or oversee the authoring of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, Pediatric Investigation Plans, and other regulatory documents
Conduct the formal review and approval of authored documents, following applicable standard operating procedures
With limited supervision, lead regulatory writing activities for complex product submissions, including new and supplemental drug applications/biologics license applications
Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)
Provide functional area input for Global Regulatory Plan and team goals
Oversee the work of contract and freelance writers train, mentor, or supervise more junior medical writers, as assigned
Lead departmental and cross-departmental initiatives, as appropriate
Generate document timeline and keep abreast of relevant professional information and technology

Fulltime

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Senior Manager/ Manager – Medical Information

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