Medical Affairs Coordinator Job at CK Group (Basingstoke)

Manager, Medical Affairs

The Manager, Medical Affairs will provide expertise as well as clinical developm...

Location

United States , Skaneateles Falls

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Minimum 5 years of related clinical experience required
industry experience preferred
Degree in related clinical field (Advanced Degree Preferred) or proven experience required
NP/PA/MD with primary and/or acute care experience such as ER, Urgent Care, or Hospitalist/internal medicine is ideal
Optometrist who displays sophisticated knowledge of physical assessment will be considered
Medical Affairs proven experience highly preferred
Active license in a U.S. state or territory in standing required with clinical expertise
Excellent written, verbal communication, and organizational skills
Effective and proficient presentation and teaching skills
Self-motivated, multi-tasking, with outstanding follow through

Job Responsibility

Serve as the medical and device subject matter expert to both internal and external customers for product development, risk assessment, training, implementation, literature reviews, and complaints
Provide accurate, balanced and timely clinical expertise to functional areas such as clinical development, R&D, marketing, manufacturing, quality assurance, regulatory affairs, and legal
Provide clinical expertise for creation and development of risk assessments and quality standards for product design history files
Devise novel approaches to address clinical and technical problems in clinical practice through development and modification of related medical devices
Assimilate voice of customer and clinical experience for design input with new product development and product lifecycle management
Develop and deliver relevant medical device training programs that support product implementation, training, and marketing efforts
Train internal customers on product application, disease states, and regional differences as required
Support product implementation process creation, maintenance, and controlled launch
Maintain familiarity of published literature as objective evidence for clinical trends and therapies related to impact on product lines
Coordinate with other Medical Partners to support Division Medical efforts.

What we offer

Comprehensive compensation and benefits packages
Medical and dental coverage starting 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) at a discount
401(k) Retirement Savings Plan with company matching
Flexible Spending Accounts
Educational assistance programs
Paid holidays and paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

Manager, Medical Affairs

The Manager, Medical Affairs will provide clinical development and technical kno...

Location

United States , Skaneateles Falls

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Minimum 5 years of related clinical experience required
industry experience preferred
Degree in related clinical field (Advanced Degree Preferred) or proven experience required
NP/PA/MD with primary and/or acute care experience such as ER, Urgent Care, or Hospitalist/internal medicine is ideal
Optometrist who displays sophisticated knowledge of physical assessment will be considered
Medical Affairs proven experience highly preferred
Active license in a U.S. state or territory in standing required with clinical expertise
Excellent written, verbal communication, and organizational skills
Effective and proficient presentation and teaching skills
Self-motivated, multi-tasking, with outstanding follow through

Job Responsibility

Serve as the medical and device subject matter expert to both internal and external customers for product development, risk assessment, training, implementation, literature reviews, and complaints
Provide accurate, balanced and timely clinical expertise to functional areas such as clinical development, R&D, marketing, manufacturing, quality assurance, regulatory affairs, and legal based on objective evidence and clinical experience
Provide clinical expertise for creation and development of risk assessments and quality standards for product design history files
Devise novel approaches to address clinical and technical problems in clinical practice through development and modification of related medical devices
Assimilate voice of customer and clinical experience for design input with new product development and product lifecycle management
Develop and deliver relevant medical device training programs that support product implementation, training, and marketing efforts
Train internal customers on product application, disease states, and regional differences as required
Support product implementation process creation, maintenance, and controlled launch when applicable
Maintain familiarity of published literature as objective evidence for clinical trends and therapies related to impact on product lines
Coordinate with other Medical Partners as needed to support Division Medical efforts

What we offer

Medical and dental coverage starting on day one
Basic life, accident, short-term and long-term disability insurance
Business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan with employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence

Fulltime

IP Legal Counsel - Medical Affairs

Reporting to the Senior Legal Counsel, the Legal Counsel will mainly provide sup...

Location

Italy , Milano

Salary:

Not provided

OPSM

Expiration Date

Until further notice

Requirements

At least 4-5 years in Intellectual Property international law firms and/or inhouse IP department, with experience in the field of medical devices and well-known consumer goods
solid expertise in intellectual property and advertising laws
medical devices regulation
Experience in review of marketing claims with a specific focus on regulated areas of advertising (medical claims/contracts with health care professional etc)
Good knowledge of Italian and European Laws and practices
Exposure to international contracting practices
Law degree in law with specialization in Intellectual Property Law and Health Law
Ability to work both independently and in a team and collaborate with cross-functional teams
Able to operate at multiple levels including with business clients, external service providers and other stakeholders
Ability to prioritize and manage multiple tasks simultaneously, strong at problem-solving and critical thinking

Job Responsibility

Revising product and marketing claims, and provide initial risk assessments and mitigation proposals under the guidance of the Senior Legal Counsel
Ensure compliance of promotional materials with local and international regulations, applying internal guidelines and best practices
Collaborate with international legal teams to implement harmonized processes and share updates
Revising and negotiating marketing contracts related to medical devices (NDA, Consultancy Agreement) for medical devices, following established templates and instructions
Provide legal support to the Senior Legal Counsel on day-to-day matters, including research, documentation, and coordination with internal stakeholders
Assist in regulatory monitoring and contribute to updating internal compliance tools

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , LA/Phoenix

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , Miami/Tampa

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , Chicago/Minneapolis

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , Cleveland/Detroit Region

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Medical Affairs Coordinator

CK Group

Location:
United Kingdom , Basingstoke

Category:
Pharmacy

Contract Type:
Contract work

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 20, 2026

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