Medical Expert Job at Launch That

Tissue Viability Nurse Expert

Harrison Associates is respected within the sector as one of the long-standing E...

Location

Salary:

Not provided

Harrisons Case Management

Expiration Date

Until further notice

Requirements

Experienced Tissue Viability Nurses with a minimum of 10 years post-qualification experience

Job Responsibility

Evaluate documentation and prepare comprehensive reports regarding the standard of care of each case
Prepare quantum reports, detailing the client's needs, your professional recommendations and associated costs
Following through the case from the initiation to completion including: timely review of new evidence and documentation, responding to queries from legal professionals, attending case conferences with barristers, participating in experts’ meetings, and writing statements as well as providing oral evidence in court if required

What we offer

A regular flow of referrals to suit your availability
Excellent remuneration and flexible hours
A self-employed contract that will work around your other work commitments
Access to a professional peer support group and continuous development
Industry-leading training package and ongoing support to all of our associates

Premarket / Postmarket Tracking Services Subject Matter Expert

The Subject Matter Expert (SME) is responsible for responding to inquiries and p...

Location

United States , Landover, MD

Salary:

Not provided

PN Automation, Inc

Expiration Date

Until further notice

Requirements

Bachelor’s degree
at least 3 years’ experience in a bio science or records management related field
Ability to abstract data from biologic applications into an Oracle or Access database and verify data or data entry or the ability to develop and implement new fileplans for records management
Proficient with office automation tools such as Adobe Acrobat Pro and other common Microsoft Windows and Microsoft Office Suite desktop applications
Thorough organizational skills, analytical skills and an astute attention to detail
Possess excellent verbal and written communication skills
Must be able to work in a fast-paced electronic production environment
Possess or be able to obtain and maintain a Government Public Trust Security Clearance

Job Responsibility

Interpret guides and manuals for processing incoming requests with numerous steps and sequences
Instructing the medical device community on sending in regulatory submissions and compiling data for the client
Resolves problems submitted by the medical device industry by analyzing issues, choosing appropriate methods to address the problems and making the necessary adjustments
Compiles data and work through issues with the internal FDA client by devising procedures or creating new processes to remedy various situations related to regulatory submissions
Analyze to ensure that the device is within the CDRH jurisdiction, that there is adequate information to proceed, whether a high priority allegation has been identified, time sensitive topics and whether a defined impact working rule applies
Investigate the request to validate the information and provide supporting sources to the request
Create request using several different applications. Be able to summarize from several different sources what the request is
Analyze and respond accordingly to incoming voicemails
Research the request and various websites to determine the correct product code
Manage allegation inbox, official correspondence and action emails

Fulltime

Senior Manager, Global Medical Affairs (Menopause)

This role is pivotal in providing subject matter knowledge and expertise, develo...

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)
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

What we offer

A fast-paced environment, with broad exposure, where you can develop professionally – even outside your area of expertise
We support you as you grow and learn, and we love to celebrate success and recognize performance
We provide opportunities for driven and talented professionals who want to be part of our exciting journey

New

Director, Medical Affairs - Osteoporosis

As an Associate Director / Director, Global Medical Affairs at Theramex, you wil...

Location

United Kingdom , London

Salary:

Not provided

Theramex

Expiration Date

Until further notice

Requirements

Qualified medical professional (Degree in Human Medicine)
Proven Medical Affairs knowledge and expertise (ideally in women’s health or related)
Leadership experience—preferably at international scale
Solid experience in healthcare professional engagement
Outstanding communication and collaboration skills
Strong business acumen
Highest ethical standards with strong command of compliance and international health authority requirements
Final ABPI signatory status
Strategic, pragmatic, and agile—thriving in fast‑paced, complex environments while delivering measurable outcomes
Passionate about women’s health and motivated to create tangible impact through science and education

Job Responsibility

Own and develop the global medical strategy for a portfolio of pharmaceutical products within the therapeutic area
Design and implement Medical Operating Plans in close collaboration with brand/product directors and other cross‑functional teams
Plan and supervise evidence generation projects (e.g., real‑world evidence)
Review and approve investigator‑initiated studies
Lead scientific publications, presentations, and dissemination of medical‑scientific data both internally and externally
Establish and maintain relationships with Global key medical experts, Healthcare providers, Academic institutions, Government agencies, Medical‑scientific societies, Advocacy groups
Create and implement engagement plans for medical‑scientific experts and patient advocacy groups
Lead advisory boards and other strategic scientific forums
Act as a senior medical‑scientific consultant to internal stakeholders, including Commercial brand teams, Regulatory Affairs, Market Access, Business Development, Other internal partners
Facilitate alignment across functions to ensure medical‑scientific integrity

What we offer

A fast‑paced environment with broad exposure, where you can grow—even beyond your area of expertise
A culture that supports continuous learning, celebrates success, and recognises high performance
Opportunities for driven, talented professionals who want to be part of our ambitious, purpose‑led journey

Manager Medical Affairs

Apex has an opportunity for an Manager Medical Affairs. Provide effective medica...

Location

United States , Acton

Salary:

35.00 - 48.00 USD / Hour

Apex Systems

Expiration Date

Until further notice

Requirements

5+ years in clinical, industry, or research settings that specifically relate to the diabetes disease state and devices (i.e., insulin pumps, continuous glucose monitors) or equivalent combination of education and experience
Life science degree with 5+ years of experience with medical affairs and/or medical strategy within medical device or pharmaceutical industry or related discipline
Proven experience in Medical Affairs including developing and leading the implementation of medical strategy
In-depth understanding of diabetes (type 1 and type 2) including disease pathophysiology, treatment options, risks, and outcomes
Advanced knowledge of diabetes technology including automated insulin delivery systems
Experience with designing research studies and interpreting data
Skilled in medical communication to diverse audience groups
Passion for working within a cross-functional team environment
Strong technical and business acumen
A clear understanding of the US and global regulatory environment related to medical devices

Job Responsibility

Provide effective medical leadership and work collaboratively within your assigned project teams to advise and guide the strategic objectives and operational decisions impacting global project direction
Act as the medical expert, drawing on your experience and knowledge of diabetes management, established standards of care, published data and key opinion leader insights
Shape medically sound product design requirements, critically assess systems and user error risks, and advise on risk control measures that ensure safe and effective use
Engage closely with clinical validation teams (Clinical Affairs, Human Factors, User Experience) to formulate study needs, evaluate outcomes, and confirmation of risk control effectiveness
Inform evidence generation strategies based on program objectives and cross functional inputs that result data needed to support regulatory approval and competitive product claims
Translate available data into meaningful and robust insights and conclusions that support regulatory requirements, commercial claims, and product value messaging
Gather and translate medical intelligence from key industry experts by engaging with the Medical Science Liaison team, investigators, and advisory boards
Collaborate on medical go to market strategies and content for regional downstream teams that include professional education programs, medical conference presentations, and other healthcare provider/customer engagements
Support assessment of professional learning needs and educational requirements that ensure safe and effective use of Omnipod and related products

What we offer

Medical, dental, vision, life, disability, and other insurance plans
ESPP (employee stock purchase program)
401K program with company match after 12 months
HSA (Health Savings Account on the HDHP plan)
SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions
Corporate discount savings program
On-demand training program
Access to certification prep and a library of technical and leadership courses/books/seminars after 6+ months
Certification discounts and other perks to associations that include CompTIA and IIBA
Dedicated customer service team

New

Director, Global Medical Affairs - Uterine Health

As an Associate Director / Director, Global Medical Affairs at Theramex, you wil...

Location

United Kingdom , London

Salary:

Not provided

Theramex

Expiration Date

Until further notice

Requirements

Qualified medical professional (Degree in Human Medicine)
Proven Medical Affairs knowledge and expertise (ideally in women’s health or related)
Leadership experience, ideally at international scale
Solid experience in healthcare professionals engagement
Outstanding communication and collaboration skills
Strong business acumen
Highest ethical standards with command of compliance and international health authorities’ requirements
Final ABPI signatory status
Strategic, pragmatic and agile operator who thrives in fast-paced, complex environments and delivers measurable outcomes
Passionate about women’s health and driven to make a tangible impact through science and education

Job Responsibility

Own and develop the global medical strategy for a portfolio of pharmaceutical products within the therapeutic area
Design and implement Medical Operating Plans in close collaboration with brand/product directors and other cross-functional teams
Plan and supervise evidence generation projects (e.g. real-world evidence)
Review and approve investigator-initiated studies
Lead scientific publications, presentations, and dissemination of medical-scientific data internally and externally
Establish and maintain relationships with global key medical experts, healthcare providers, academic institutions, government agencies, medical-scientific professional societies and advocacy groups
Create and implement key medical-scientific experts and patient advocacy groups engagement plans
Lead advisory boards and other strategic scientific forums
Act as a senior medical-scientific consultant to internal stakeholders, including commercial brand teams, regulatory affairs, market access, business development, other
Facilitate alignment across functions to ensure medical-scientific integrity

What we offer

A fast-paced environment with broad exposure, where you can grow—even beyond your area of expertise
A culture that supports continuous learning, celebrates success, and recognizes performance
Opportunities for driven, talented professionals who want to be part of our ambitious, purpose-led journey

Industrial Disease Fee Earner

An Industrial Disease or Personal Injury Fee Earner is wanted for an excellent o...

Location

United Kingdom , Castleford

Salary:

25000.00 - 45000.00 GBP / Year

Douglas Scott

Expiration Date

Until further notice

Requirements

Industrial disease or personal injury experience
Ability to manage cases from inception to settlement
Providing expert legal advice
Liaising with medical professionals
Negotiating settlements

Job Responsibility

Handle a varied caseload of industrial disease claims
Manage cases from inception to settlement
Provide expert legal advice
Liaise with medical professionals
Negotiate settlements on behalf of clients

What we offer

Market leading benefits package
Remote and flexible working

Fulltime

Industrial Disease Fee Earner

An Industrial Disease or Personal Injury Fee Earner is wanted for an excellent o...

Location

United Kingdom , Leeds

Salary:

30000.00 - 50000.00 GBP / Year

Douglas Scott

Expiration Date

Until further notice

Requirements

Prior industrial disease experience
Experience in personal injury fee earning
Ability to manage cases from inception to settlement
Providing expert legal advice
Liaising with medical professionals
Negotiating settlements on behalf of clients

Job Responsibility

Handle a varied caseload of industrial disease claims
Manage cases from inception to settlement
Provide expert legal advice
Liaise with medical professionals
Negotiate settlements on behalf of clients

What we offer

Market leading benefits package
Remote and flexible working

Fulltime

Medical Expert

Launch That

Location:
United States

Category:
Media

Contract Type:
B2B

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 09, 2025

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Job Description:

Job Responsibility:

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Job Posted:December 09, 2025

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Location:
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Contract Type:
B2B

Job Posted:
December 09, 2025