Medical Science Liaison or Senior Medical Science Liaison Job at BioMarin Pharmaceutical

New

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 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

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

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

Key Account Manager aHUS

Proclinical is seeking a Key Account Manager to join a dynamic team focused on r...

Location

Germany , München

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Background in biotechnology or pharmaceutical sales, preferably in the orphan market
Master's degree in biology, Chemistry, or a related field with a strong sales mindset
Ability to work independently and collaboratively in a team-oriented environment
Experience in managing scientific events and projects
Strong relationship-building skills with healthcare providers in both community and academic settings
Effective presentation and communication skills with the ability to address customer needs and concerns
Flexibility to work across different indications and target groups as required
Proficiency in Microsoft Office tools (Outlook, PowerPoint, Word, Excel) and reporting systems
Knowledge of pharmaceutical regulations in the country
Willingness to travel regularly within the territory, including overnight stays

Job Responsibility

Build and maintain relationships with office-based and hospital nephrologists, pharmacists, nurses, and other relevant healthcare professionals
Develop a positive image of the company among key customer groups
Analyze the region to identify and develop centers specializing in rare diseases in nephrology
Provide educational and commercial services to physicians and pharmacies
Promote products in alignment with marketing and sales strategies while adhering to legal and compliance guidelines
Plan, organize, and execute local educational sessions for healthcare professionals
Collaborate cross-functionally with marketing, medical science liaisons, and other teams to ensure cohesive account management
Maintain accurate records in the CRM database and provide timely reporting to senior management
Collect and report pharmacovigilance information as per internal procedures
Represent the territory in reviews, account planning discussions, and at national/international events and congresses

Fulltime

Senior Clinical Research Associate

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

Location

United States , Remote

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, CRAs are 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 (site quality/performance) within the LST
Drives performance at the sites
Updates CTMS and other systems with data from study sites as per required timelines

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

New

Senior Director, Field Market Access

We’re seeking a dynamic Head of Field Market Access to lead the field market acc...

Location

Salary:

260000.00 - 320000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor's degree required
advanced degree preferred
18+ years of progressive experience in the pharmaceutical or biotech industry
10+ years in market access, including field and / or strategy roles
5+ years of people leadership experience
Rare disease or oncology experience required
buy & bill experience required
Cell or Gene Therapy experience preferred
Deep understanding of: Commercial payers (national and regional) and approach to medical policy decision-making
Medicaid policy development

Job Responsibility

Lead team responsible for all market access and reimbursement stakeholder field engagement for assigned accounts (payer and Treatment Center)
Serve as a subject matter expert on local payers (Medicaid and commercial), including payer needs, policy shifts, and contracting opportunities
Support team in delivering compelling value propositions and payer materials customized to each stakeholder’s needs
Help team build and execute account-specific business plans in alignment with Beam’s broader market access and brand strategies
Partner cross-functionally with other field leadership, including Medical Science Liaisons and Key Account Management teams, especially for Treatment Center engagement
Track and report market trends, competitive intelligence, policy changes, and access barriers across the commercial self-insured and Medicare landscapes
Collaborate on the development of performance KPIs and metrics to evaluate access success and account performance

Fulltime

Senior Compliance Engineer

We are seeking a highly motivated and experienced Senior Compliance Engineer to ...

Location

United States , Pleasanton

Salary:

Not provided

10x Genomics

Expiration Date

Until further notice

Requirements

Minimum of Bachelor’s degree in Electrical Engineering or related engineering field
10+ years of experience in regulatory compliance for hardware products, reagents, or both—preferably within the life sciences, diagnostics, or medical device industries
Additional Experience with chemical and reagent compliance, including SDS authoring, GHS/CLP labeling, and familiarity with REACH, TSCA, and international chemical inventory regulations is strongly preferred
Familiarity with environmental regulations (RoHS, REACH, WEEE, TSCA, etc.) and how they apply to product design, component selection, and global distribution
Strong project management skills, with the ability to manage multiple regulatory timelines and interact with cross-functional teams (e.g., R&D, manufacturing, supply chain)
Excellent technical writing and documentation skills, including experience with compliance reports, regulatory submissions, and audit-ready file maintenance
Ability to interpret regulatory language and apply it practically to product development and compliance strategies

Job Responsibility

Collaborating with a cross-functional team to ensure compliance to regulatory requirements including UL, CSA, FCC, CE, KCC, SRRC, PSE, CB
Submitting official certification through relevant compliance bodies such as FCC, CE, UL, TUV, KCC, MIC, SRRC, etc. and acting as a liaison between 10x Genomics and state, local, federal and international agencies to submit required forms and paperwork while maintaining date and files for future reference, particularly in the event of an audit by a regulatory agency
Understanding RoHS, REACH, TSCA, Waste Electrical and Electronic Equipment (WEEE) Regulation and ensuring that new and existing products are designed to comply with those guidelines and tested accordingly
Determining and interpreting the relevant regulatory standards such as IEC 61010-1, IEC 61010-2-010, IEC 61010-2-081, IEC 60601 and how they apply to 10x Genomics products to establish and maintain guidelines and best design practices to mitigate compliance issues early in the design phase
Partner with R&D to ensure compliance with global EMC and EMI regulatory requirements, and working closely with electrical and systems engineering teams to define and implement design guidelines for shielding, grounding, and layout strategies to reduce emissions and improve immunity
Staying up to date with any changes to global agency approvals and testing procedures, as well as reviewing marketing, legal and technical documentation (for example: labeling user guides and declaration of conformity) to assess compliance with regularly reporting on compliance status and measures to both internal and external parties
Maintaining a deep understanding of new and existing regulation that may impact 10x Genomics products and processes and using that understanding to standardize all business operations and establish clearly documented protocols while explaining regulations, procedures and policies to all employees and stakeholders as necessary
Preparing Manufacturing site ready for the Regulatory Body audit for Product Safety Certification. Establishing a routine manufacturing test equipment Program for Hipot & Ground Bond testing, and managing bi-annual audits with external regulatory agencies for Product Safety Certification

What we offer

Health Package
Easy-to-use Benefits
Family oriented policies like parental leave
Generous Time Off

Medical Science Liaison or Senior Medical Science Liaison

BioMarin Pharmaceutical

Location:
United States

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 17, 2026

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