Medical Science Liaison Jobs

Medical Science Liaison

As a Medical Science Liaison, you will advance medical science through clinical ...

Location

Algeria , Algiers

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Excellent product knowledge and expertise
Outstanding presentation and communication skills in both the local language and English
Proven teaching capabilities and an understanding of adult learning concepts
Effective critical thinking skills and strategy implementation
A broad understanding of the regulatory and healthcare environment in the country/region
Excellent organizational skills, resilience, and empathy
An MD and/or PhD and/or equivalent healthcare qualifications, preferably with proven MSL experience
2-3 years post-graduate experience within the healthcare industry
Clinical trial experience with knowledge of GCP
Training in adverse event reporting

Job Responsibility

Identifies and advances clinical needs, ensuring that we continually meet the evolving requirements of the healthcare community
Acts as the primary contact for investigator-initiated trials, facilitating the successful implementation of research initiatives
Assists in the development of publication plans to share new findings and insights with the broader medical community
Supports the medical manager in the review of promotional materials, ensuring they comply with the highest standards of accuracy and compliance
Acts as a liaison with the medical community, including medical professional societies, opinion leaders, investigators, and consultants
Supports the medical director/medical manager in collaborating with opinion leaders
Provides accurate and balanced medical-scientific education and information on products, therapies, issues, trends, and clinical research
Conducts demonstrations and in-services at customer sites
Assists in the development of medical-scientific advisory boards, symposia, and educational forums
Educates and trains internal staff on products and therapies

Fulltime

Medical Science Liaison

As a MEDICAL SCIENCE LIAISON in Algeria at Baxter you will play a pivotal role i...

Location

Algeria , Algiers

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Excellent product knowledge and expertise
Outstanding presentation and communications skills in both the local language and English
Proven teaching capabilities and an understanding of adult learning concepts
Effective critical thinking skills and strategy implementation
A broad understanding of the regulatory and healthcare environment in the country/region
Excellent organizational skills, resilience, and empathy
An MD and/or PhD and/or equivalent healthcare qualifications, preferably with proven MSL experience
2-3 years post-graduate experience within the healthcare industry
Clinical trial experience with knowledge of GCP
Training in adverse event reporting

Job Responsibility

Identifies and advances clinical needs, ensuring that we continually meet the evolving requirements of the healthcare community
Acts as the primary contact for investigator-initiated trials, facilitating the successful implementation of research initiatives
Assists in the development of publication plans to share new findings and insights with the broader medical community
Supports the medical manager in the review of promotional materials, ensuring they compete with the highest standards of accuracy and compliance
Acts as a liaison with the medical community, including medical professional societies, leaders with a point of view, visionaries, investigators, and consultants
Supports the medical director/medical manager in collaborating with leaders with a point of view, encouraging relationships that drive innovation and excellence in medical science
Provides accurate and fair-balanced medical-scientific education and information on products, therapies, issues, trends, and clinical research
Conducts demonstrations and in-services at customer sites to ensure flawless clinical use of products
Assists in the development of medical-scientific advisory boards, symposia, and other educational forums
Educates and trains internal staff on products, therapies, issues, trends, and clinical research, ensuring our team remains at the forefront of medical knowledge

Fulltime

New

Data Scientist

Medical Data Scientist will play a vital role in supporting Global Medical Affai...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

PhD in Computer Science, Engineering, Statistics, or a related quantitative field and 1+ year(s) of experience in data analytics or data science
OR, Master’s degree in Computer Science, Engineering, Statistics, or a related quantitative field and 3+ years of experience in data analytics or data science
OR, Bachelor’s degree in Computer Science, Engineering, Statistics, or a related quantitative field and 5+ years of experience in data analytics or data science
Experience in data science, statistics, machine learning, or advanced analytics, with hands-on application of statistical techniques such as hypothesis testing, regression analysis, clustering, and classification
Working knowledge of SQL and Python (R a plus)
comfort working in Databricks or similar environments
Passion for applying technical skills to solve complex business problems and drive data-driven transformation

Job Responsibility

Support the application of data science methods — including advanced statistical techniques, predictive modeling, and machine learning — to design, develop, and deploy solutions that address complex medical questions across therapeutic areas
Support and execute components of data science projects across structured and unstructured datasets (e.g., HCP sentiment, scientific engagement data, publications, CRM/field medical data) using Python, R, SQL, Tableau, Power BI, or similar platforms
Assist in designing and evaluating experimentation and pilots (e.g., digital channel optimization or field medical targeting) to test innovative approaches, with a focus on scaling successful solutions
Work in technical teams and contribute to medical data science projects such as Medical Science Liaison (MSL) engagement optimization, MSL note sentiment analysis using LLMs, and digital engagement impact measurement, turning complex data into insights that enable more effective field medical activities
Support building and optimizing scalable data pipelines for ingestion, cleansing, transformation, model training, automation, and deployment in partnership with data engineering and platform teams
Collaborate with cross-functional stakeholders (Medical, Commercial, and Technology groups across Amgen India) to ensure analyses directly address key medical business questions and strategic priorities
Partner with data science, IT, and external vendors to support data access, integrity, and governance
Help to translate analytic outputs into clear, actionable insights and recommendations and deliver compelling presentations, reports, and visualizations to medical and cross-functional leadership teams
Stay curious — continuously learn and apply emerging methods such as LLMs, Generative AI, A/B testing, and causal inference to strengthen analytical approaches
Support documentation, version control, and deployment practices using standardized platforms and tools

What we offer

Competitive salary and comprehensive benefits package
Opportunities for professional growth and career development
A collaborative and inclusive work environment

Fulltime

Program Coordinator

Support Account Team for Successful Project Delivery. Provide team members with ...

Location

India , Remote; Hyderabad; Bengaluru

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Competent in the use of Word (Advanced), PowerPoint (Advanced), Excel (Advanced), Outlook (Advanced) and Reference Manager (Intermediate) and sound knowledge of databases (eg, Access)
Ability to source information using the Internet and other media
Confident processing financial information and trackers under the guidance of Manager
A confident self-starter who is capable of knowing how best to action/respond to specific requests and information received from a variety of external and internal sources
Strong interpersonal and communications skills, including ability to compose own correspondence to agree professional standard
Excellent organizational and multi-tasking skills, with the ability to coordinate several projects at different stages, meeting strict deadlines and follow-up proactively
effective time management
Accuracy and attention to detail
Team player with client-focused approach
Motivated, proactive, flexible approach, with ability to follow tasks to completion

Job Responsibility

Support Account Team for Successful Project Delivery
Provide team members with skilled support in the implementation and management of specified projects within agreed time schedules and budgets
Proactively maintain and circulate project tracking and status reports, internally (including liaison with the studio) and externally
Set up and maintain accurate project information on all tracking tools (internal and external)
Set-up project (status reports, tracking documents, document naming convention) and project codes
Prepare project kick off materials, including creating project job sheet
Raise purchase orders for all external services (ICs) as per standard processes and procedures with authorization by an appropriate signatory
track payments
Generate appropriate correspondence when seeking permission to reproduce illustrations/figures
Undertake ordering of Journal/British Library held references

What we offer

Benefits vary by country, but Parexel is passionate about our team’s overall wellness
We believe that investing in your professional and personal development is an investment in Parexel, and we want to help you realize your full potential and career

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

New

Clinical Site Relationship Manager

TFS HealthScience is a leading mid-sized Contract Research Organization (CRO) de...

Location

United States , Houston; Durham; Gaithersburg; Miami; Washington, D.C.; San Diego; Raleigh

Salary:

Not provided

TFS HealthScience

Expiration Date

Until further notice

Requirements

Bachelor's degree in a relevant field (life sciences, nursing, healthcare management)
Proven experience in clinical research and site relationship management
Excellent communication and interpersonal skills
Proactive problem-solving abilities
Strong organizational and project management skills
Solid understanding of GCP and regulatory requirements

Job Responsibility

Relationship Building: Develop and maintain strong relationships with key personnel at clinical trial sites, including principal investigators, site coordinators, and other site staff
Liaison Role: Serve as a bridge between the sponsor and clinical trial sites, ensuring clear and timely communication of study protocols, updates, and key information
Site Oversight: Conduct Monitoring Oversight Visits and regular site engagement activities to ensure high-quality trial execution
Enrollment Support: Design customized site-level engagement plans to help drive enrollment and support timely patient recruitment
Issue Resolution: Collaborate with CRO CRAs and Medical Science Liaisons to identify, mitigate and resolve site-level challenges
Feasibility Support: Participate in feasibility and site qualification visits, collaborating with CRO representatives
Advocacy Engagement: Represent the sponsor at local and regional patient advocacy or support group meetings when needed
Reporting: Track and report site engagement activities, enrollment status, and performance metrics

Fulltime

Medical Social Work Supervisor

Under general supervision, the Medical Social Work Supervisor oversees recruitme...

Location

United States , San Francisco

Salary:

124514.00 - 151346.00 USD / Year

City and County of San Francisco

Expiration Date

Until further notice

Requirements

Four (4) years of post-Master's Medical Social Worker experience in a health care setting
Current licensure as a Clinical Social Worker (LCSW) issued by the State of California Board of Behavioral Sciences as required under Title 22, California Administrative Code, Section 70055

Job Responsibility

Oversees recruitment, training, supervision, and evaluation of social work staff
Assigns caseloads
Provides clinical consultation and supervision on complex cases
Coordinates medical social services programs
Performs therapy
Handles administrative duties
Participates in hospital and community activities
Supervises assigned personnel
Provides consultation concerning the most difficult/complex cases
Manages complex cases as needed

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
Ability to work in an environment of remote collaborators
Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials
Good analytical and problem-solving skills
Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines

Job Responsibility

Contributes to the selection of potential investigators
Accountable for study start-up and regulatory maintenance (in some countries)
Trains, supports, and advises Investigators and site staff in study related matters
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
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
Drives performance at the sites
Proactively identifies and ensures timely resolution to study-related issues
Updates CTMS and other systems with data from study sites

What we offer

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

Medical Science Liaison

Amgen

Location:
Japan, Tokyo

Category:
-

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 18, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Medical Science Liaison

Medical Science Liaison

Medical Science Liaison

Data Scientist

Program Coordinator

Senior Clinical Research Associate

Clinical Site Relationship Manager

Medical Social Work Supervisor

Senior Clinical Research Associate

Medical Science Liaison

Amgen

Location:Japan, Tokyo

Category:-

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:December 18, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Medical Science Liaison

Medical Science Liaison

Medical Science Liaison

Data Scientist

Program Coordinator

Senior Clinical Research Associate

Clinical Site Relationship Manager

Medical Social Work Supervisor

Senior Clinical Research Associate

Location:
Japan, Tokyo

Category:
-

Contract Type:
Not provided

Job Posted:
December 18, 2025