Senior Medical Science Liaison Job at Kailera Therapeutics

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
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
Serve as a medical/scientific resource through answering unsolicited medical questions
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 site identification and evaluation, recruitment, investigator meetings, external expert identification, and study management
Support clinical operations in identifying and interacting with potential investigators

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

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

Medical Science Liaison

We are partnering exclusively with a specialist pharmaceutical company building ...

Location

United Kingdom

Salary:

Not provided

CK Group

Expiration Date

Until further notice

Requirements

A life sciences or medical background (e.g. pharmacy, biomedical science, medicine or similar)
Previous experience in a UK customer-facing Medical Affairs role (MSL, Senior MSL or equivalent)
Strong understanding of the UK NHS, particularly specialist or tertiary care pathways
Experience engaging with cardiology, lipid, metabolic, endocrinology or rare disease stakeholders
Proven ability to communicate complex scientific data clearly, confidently and compliantly
A proactive, autonomous working style with strong insight-generation capability
It is essential that applicants hold entitlement to work in the UK

Job Responsibility

Building and maintaining strong, credible relationships with KOLs, specialist clinicians, and academic experts
Leading scientific exchange on rare lipid and metabolic disease, including disease pathways, clinical evidence and patient management
Delivering medical education and disease awareness initiatives aligned to the medical strategy
Capturing and communicating actionable insights to inform medical, evidence-generation and cross-functional planning
Supporting launch and post-launch activities, including advisory boards, congresses and expert meetings
Contributing to evidence-generation activities such as registries, real-world evidence, non-interventional studies and investigator-initiated research
Working closely with Medical Affairs, Market Access and Commercial colleagues to support aligned, compliant decision-making

What we offer

Competitive salary and benefits package

Fulltime

Director, Senior Medical Science Liaison

Senior Medical Science Liaisons (MSL) will be key members of the Field Medical A...

Location

United States

Salary:

175000.00 - 230000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

6+ years of pharmaceutical/biotechnology industry experience or relevant experience
MSL experience strongly preferred
Deep scientific knowledge and genuine passion for obesity medicine, metabolism, endocrinology, or related therapeutic areas
Prior experience in supporting clinical trial site engagement and early development programs
Demonstrated ability to understand, interpret, and communicate complex clinical and scientific data
Excellent presentation, communication, interpersonal, and cross-functional collaboration skills
Strong strategic thinking and problem-solving abilities
Ability to work independently in a dynamic, fast-paced environment with minimal supervision
Willingness to travel up to 60-80% (primarily within assigned territory)
Valid driver's license and ability to travel by car and air

Job Responsibility

Develop and maintain a strategic and comprehensive territory plan for engagement with top key opinion leaders, investigators, centers of excellence, Health Systems and professional societies in obesity medicine and related therapy areas
Establish and maintain peer-to-peer relationships with key opinion leaders, key decision makers, clinical investigators, and healthcare professionals in obesity medicine and related therapy areas
Serve as subject matter expert at key medical and scientific conferences, advisory boards, roundtables, clinical investigator meetings, speaker trainings, and internal meetings
Deliver scientifically balanced, evidence-based presentations on Kailera's pipeline, disease state, products, and emerging data
Respond to unsolicited medical information requests with accuracy and compliance. Proactively identify health care professional educational needs and address with fair balanced tailored responses
Consistently execute on the current Medical Affairs strategy and field medical priorities
Support clinical trial site identification, feasibility assessment, and investigator engagement
Provide scientific support to active and potential clinical trial sites
Facilitate communication between clinical operations teams and investigators
Monitor and report competitive intelligence and disease landscape insights from the field

What we offer

comprehensive health coverage
flexible time off
paid holidays
year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

Onc hematology field mas

The MAS role family comprises a variety of medical scientific specialties, such ...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

4 year university undergraduate degree AND master’s degree in life science
Pharmacists 4-year university graduates with pharmacist license and master’s degree or above or equivalent life science research experience
6–year university graduates with pharmacist license
Nurses with master’s degree or above
Veterinarians
Dentists
MDs
Medical/ pharmaceutical expert knowledge of therapeutic disease area/ products
Ability to communicate appropriately and build good relationship with internal/external stakeholders
Work effectively with teams and across functions by demonstrate Pfizer’s Values & Behaviors and the agility to learn from others

Job Responsibility

Demonstrate medical and scientific leadership and expertise
Provide and exchange medical/ scientific information for/from medical institutions (and other related sources) in the assigned area and from stakeholders
Drive for heightened understanding of the clinical and medical attributes of our products
Maintain the highest scientific standards during in/ external activities
Contribute to the implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines / vaccines
Make important contributions to decisions of medical strategies for assigned products
Contribute to achieving the department/team goals, and/or participate in cross-organizational projects
Play an active role in supporting members in the team/organization
Develop and execute the medical plan aligned with the medical strategy
Identify unmet medical needs and healthcare disparities in the assigned asset(s) and therapeutic area(s)

Fulltime

Amyloidosis, Medical Affairs Scientist

The MAS role family comprises a variety of medical scientific specialties, such ...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Minimum requirement: 4 year university undergraduate degree AND master’s degree in life science, or Pharmacists 4-year university graduates with pharmacist license and master’s degree or above or equivalent life science research experience, or 6–year university graduates with pharmacist license, or Nurses with master’s degree or above, or Veterinarians, or Dentists, or MDs
Preferred: In addition to those who meet the minimum requirements above, the qualifications below are preferred MD (clinical experience, board certification preferred), or PhD in Life Science
Technical Skills: Medical/ pharmaceutical expert knowledge of therapeutic disease area/ products
Ability to communicate appropriately and build good relationship with internal/external stakeholders
Work effectively with teams and across functions by demonstrate Pfizer’s Values & Behaviors and the agility to learn from others
Capable of medical discussion with relevant departments and external HCPs.
A person who understands compliance and relevant laws/regulations in the pharmaceutical industry and advocates the appropriate use of the products.
Can demonstrate appropriate knowledge and understanding of internal organization structure, key stakeholders and strategies
A person who is able to quickly acquire necessary medical/ scientific knowledge and skills though self-learning
Experience: Work experience at functions of: Medical Affairs

Job Responsibility

Demonstrate medical and scientific leadership and expertise
Provide and exchange medical/ scientific information for/from medical institutions (and other related sources) in the assigned area and from stakeholders.
Drive for heightened understanding of the clinical and medical attributes of our products in order to enhance the safe and efficacious use.
Maintain the highest scientific standards during in/ external activities to provide deep medical and scientific expertise.
Contribute to the implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines / vaccines to address unmet medical needs and fill data gaps.
Make important contributions to decisions of medical strategies for assigned products, in order to ensure safe, proper, and effective use of assigned products.
Contribute to achieving the department/team goals, and/or participate in cross-organizational projects as a core member and provide guidance to deliver the results.
Play an active role in supporting members in the team/organization with the line manager to move towards its goals
Develop and execute the medical plan aligned with the medical strategy to meet unmet medical needs in the assigned product(s) and therapeutic area(s) in collaboration with office medical
Identify unmet medical needs and healthcare disparities in the assigned asset(s) and therapeutic area(s) through medical activities such as advisory board meetings and scientific exchanges with HCPs and other relevant individuals and organizations.

Fulltime

Dermatology, MAS(Field) Manager

The MAS role family comprises a variety of medical scientific specialties, such ...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

4 year university undergraduate degree AND master’s degree in life science
Pharmacists 4-year university graduates with pharmacist license and master’s degree or above or equivalent life science research experience
6–year university graduates with pharmacist license
Nurses with master’s degree or above
Veterinarians
Dentists
MDs
Medical/ pharmaceutical expert knowledge of therapeutic disease area/ products
Ability to communicate appropriately and build good relationship with internal/external stakeholders
Work effectively with teams and across functions by demonstrate Pfizer’s Values & Behaviors and the agility to learn from others

Job Responsibility

Collaborate with medical stakeholders as a scientific expert for HCPs, medical societies, academia, and other relevant organizations
Establish a strong collaborative scientific relationship through non-promotional activities such as scientific exchanges with relevant stakeholders in dermatology
Develop and maintain a comprehensive stakeholder map
Handle UMR (Unsolicited Medical Request) responses
Follow up clinical investigator-sponsored research and medical grants compliant with Pfizer policies
Acquire extensive medical/pharmaceutical information and gather the latest medical information
Deliver key medical and scientific activities within the medical plan
Provide and exchange medical/ scientific information for/from medical institutions and from stakeholders
Drive for heightened understanding of the clinical and medical attributes of our products
Maintain the highest scientific standards during in/ external activities

Fulltime

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Excellent attention to detail
Good written and verbal communication skills
Good collaboration and interpersonal skills
Good negotiation skills
Proficient in written and spoken English language required
Fluency in local language(s) required
Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
Good knowledge of relevant local regulations
Good medical knowledge and ability to learn relevant Client Therapeutic Areas
Basic understanding of the drug development process

Job Responsibility

Contributes to the selection of potential investigators
In some countries, as required, accountable for study start-up and regulatory maintenance
Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles
Confirms that site staff have completed and documented the required training appropriately
Actively participates in Local Study Team (LST) meetings
Contributes to National Investigators meetings, as applicable
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
Shares information on patient recruitment and study site progress
Drives performance at the sites
Proactively identifies and ensures timely resolution to study-related issues

What we offer

Patient-focused in everything we do
Supportive and inclusive environment
Career growth and development
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

Senior Medical Science Liaison

Kailera Therapeutics

Location:
United States

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 03, 2026

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