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Clinical Science Manager Jobs (NOW HIRING)

Advita Ortho

Clinical Science Manager

Gainesville, FL · On-site

Clinical Science Manager Department: Clinical Employment Type: Full Time Location: Gainesville, FL Reporting To: Chief Quality, Regulatory, & Clinical Officer Description This position is responsible ...

Exactech

Clinical Science Manager

Gainesville, FL

This position is responsible for facilitating the strategic planning and coordination of the Clinical Science team and ensuring high-quality medical writing and research services. The role manages ...

Exelixis

Senior Clinical Science Manager

Alameda, CA · On-site

$139K - $197K/yr

Maintain clinical and technical writing expertise in the therapeutic area of Oncology; review scientific journals, attend scientific and key technical meetings as warranted. * Collaborate with team ...

Exelixis

Senior Clinical Science Manager

Alameda, CA

$139K - $197K/yr

Maintain clinical and technical writing expertise in the therapeutic area of Oncology; review scientific journals, attend scientific and key technical meetings as warranted. Collaborate with team ...

Exelixis

Senior Clinical Science Manager

Alameda, CA · On-site

$139K - $197K/yr

... clinical and technical writing expertise in the therapeutic area of Oncology; review scientific journals, attend scientific and key technical meetings as warranted. • Collaborate with team members ...

Telix Pharmaceuticals (AMER)

OR

Provide senior management personnel regular updates on the progress of the clinical research ... Scientific background with university degree and MD required * 10+ years Clinical experience with ...

Natera

Director, Clinical Science

$81K - $111K/yr

Collaborate with data management teams to write Data Review Plans, track trial outliers, and audit ... Mentor and develop junior clinical science personnel, implementing process optimizations across ...

Natera

OR

$79K - $108K/yr

Collaborate with data management teams to write Data Review Plans, track trial outliers, and audit ... Mentor and develop junior clinical science personnel, implementing process optimizations across ...

Natera

Director, Clinical Science

San Carlos, CA

$96K - $131K/yr

Collaborate with data management teams to write Data Review Plans, track trial outliers, and audit ... Mentor and develop junior clinical science personnel, implementing process optimizations across ...

Bayer

Clinical Science Lead

Boston, MA · On-site

$136K - $204K/yr

... Manage studies and provide scientific input to operational colleagues, external parties, and study ... clinicians and scientists to drive the development of a robust pipeline WHO YOU ARE Bayer seeks an ...

Olema Oncology

Director, Clinical Science

Boston, MA · On-site

$220K - $245K/yr

... Management, Biostatistics, Clinical Pharmacology, Regulatory and Program Management, in the ... Attending scientific meetings pertinent to clinical science activities And will also include:

New

Olema Oncology

Director, Clinical Science

Boston, MA · On-site

$86K - $118K/yr

... Management, Biostatistics, Clinical Pharmacology, Regulatory and Program Management, in the ... Attending scientific meetings pertinent to clinical science activities And will also include:

Bayer Inc.

Clinical Science Lead

Cambridge, MA

$136K - $204K/yr

Clinical Science Lead As a Clinical Science Lead, you will be a key figure in leading the clinical ... Manage studies and provide scientific input to operational colleagues, external parties, and study ...

Bayer

Clinical Science Lead

Cambridge, MA

$136K - $204K/yr

... Manage studies and provide scientific input to operational colleagues, external parties, and study ... clinicians and scientists to drive the development of a robust pipeline WHO YOU ARE Bayer seeks an ...

Bayer

Clinical Science Lead

Cambridge, MA · On-site

$136K - $204K/yr

Clinical Science Lead As a Clinical Science Lead, you will be a key figure in leading the clinical ... Manage studies and provide scientific input to operational colleagues, external parties, and study ...

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Clinical Science Manager information

See salary details

$43.5K

$82.3K

$140K

How much do clinical science manager jobs pay per year?

As of Jun 29, 2026, the average yearly pay for clinical science manager in the United States is $82,350.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $89,500.00 per year, depending on experience, location, and employer.

How does a Clinical Science Manager typically collaborate with cross-functional teams during clinical trial development?

Clinical Science Managers play a key role in bridging scientific objectives with operational execution by working closely with clinical operations, regulatory affairs, data management, and medical affairs teams. They often lead the development of clinical protocols and ensure scientific integrity throughout the study, facilitating regular meetings and communication to align project goals and timelines. Their collaborative efforts help anticipate and resolve challenges, streamline processes, and ensure that trials meet regulatory requirements and scientific standards.

What are Clinical Science Managers?

Clinical Science Managers are professionals who oversee and coordinate clinical research projects, often within the pharmaceutical, biotechnology, or medical device industries. They are responsible for managing clinical trials, ensuring regulatory compliance, and collaborating with cross-functional teams such as clinical operations, regulatory affairs, and medical affairs. Their role involves protocol development, data analysis, and ensuring the safety and efficacy of investigational products. Clinical Science Managers also play a critical part in interpreting study results and presenting findings to stakeholders. They typically have advanced degrees in life sciences and significant experience in clinical research.

What is the difference between Clinical Science Manager vs Clinical Research Associate?

AspectClinical Science ManagerClinical Research Associate
CredentialsTypically requires advanced degrees (e.g., Master’s or PhD) and industry experienceUsually holds a bachelor’s degree in life sciences or related field
Work EnvironmentLeads teams, manages projects, and oversees clinical studiesMonitors clinical trials at sites, ensures protocol compliance
Employer & Industry UsagePharmaceutical, biotech, and medical device companiesContract research organizations, pharmaceutical companies
Search & Comparison IntentUnderstanding managerial roles in clinical scienceFocus on trial monitoring and site management

The Clinical Science Manager typically oversees clinical projects and manages teams, requiring advanced credentials. In contrast, the Clinical Research Associate focuses on monitoring clinical trials at sites. Both roles are essential in the clinical research process but differ in responsibilities and experience levels.

What are the key skills and qualifications needed to thrive as a Clinical Science Manager, and why are they important?

To thrive as a Clinical Science Manager, you need a solid background in clinical research, life sciences, and project management, typically supported by an advanced degree (e.g., PharmD, PhD, or MD) and industry experience. Familiarity with clinical trial management systems, regulatory compliance tools, and data analysis platforms is crucial. Strong leadership, strategic thinking, and effective communication skills help you manage cross-functional teams and build relationships with stakeholders. These competencies ensure the successful design, execution, and oversight of clinical studies, ultimately advancing scientific and business goals.
More about Clinical Science Manager jobs
What cities are hiring for Clinical Science Manager jobs? Cities with the most Clinical Science Manager job openings:
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Clinical Science Manager jobs near you
Infographic showing various Clinical Science Manager job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, 7% Part Time, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $82,350 per year, or $39.6 per hour.

Clinical Science Manager

Advita Ortho

Gainesville, FL • On-site

Full-time

Posted 18 days ago

Key responsibilities

  • Oversee the management and implementation of assigned Clinical Science projects, ensuring alignment with company goals.

  • Lead cross-functional project teams in planning and executing pre-clinical and clinical studies, and maintain strong relationships with team members and stakeholders.

  • Prepare and submit scientific publications, clinical evaluation reports, and literature reviews while ensuring compliance with FDA and international standards.

Job description

Clinical Science Manager
Department: Clinical
Employment Type: Full Time
Location: Gainesville, FL
Reporting To: Chief Quality, Regulatory, & Clinical Officer
Description
This position is responsible for facilitating the strategic planning and coordination of the Clinical Science team and ensuring high-quality medical writing and research services. The role manages and develops cross-functional project teams and maintains strong
relationships with various stakeholders
Key Responsibilities
  • Oversee the management and implementation of assigned projects. This includes leveraging and expanding experience for future project assignments and developing strategies that align with the company's goals.
  • Act as the liaison and primary point of contact for all Clinical Science related issues across Advita's global businesses.
  • Lead specified BU cross-functional project teams in planning and executing pre-clinical and clinical studies. These studies should align with scientific claims and include strategies for preclinical study, clinical research, publication, and marketing communication.
  • Establish, develop, and maintain strong working relationships with cross-functional project team members. Coordinate and supervise the activities performed by the Clinical Science team.
  • Facilitate early engagement of key surgeon investigators in research strategies.
  • Drive the preparation and submission of scientific publications (white papers, abstracts, manuscripts) aligned with claims strategies. Manage publication submission timing to align with key annual scientific meetings/conferences.
  • Manage Clinical Science deliverables in collaboration with Regulatory, Quality, Engineering, and business leaders.
  • Educate and mentor team members on medical writing and research best practices.
  • Prepare clinical evaluation reports for regulatory submissions, perform data analysis of clinical outcomes, and conduct literature reviews. Ensure compliance with FDA and international standards, including Design Control and Risk Management processes.
  • Support risk/benefit analyses conducted by Engineering. Participate in complaint handling, corrective and preventive action, and internal quality audit processes. Provide knowledge and support to operate within company and regulatory guidelines.
  • Independently manage multiple medium to large-scale writing/research projects. Ensure that company procedures, processes, and documentation meet required guidelines for maintaining FDA compliance and ISO/EC/CMDR certification.
  • Work collaboratively with other functional areas to feed back the analysis of post-market information into Risk
  • Management and the Design and Development process. Assist and support other employees, teams, and sales personnel as necessary.
  • Apply the Quality System and relevant Federal and International standards effectively.
  • Lead the Clinical Science team

Skills Knowledge and Expertise
Education:
  • Bachelor's Degree in a related field from an accredited institution required; Master's Degree preferred

Experience:
  • Five (5) years of experience in medical writing or similar field
  • Medical/Technical writing skills required
  • Experience in systematic literature review required
  • Experience in medical devices preferred
  • US and EU clinical trial experience
  • Experience in pre-market and post market

Functional/Technical Knowledge, Skills and Abilities Required:
  • Detail oriented and strong organizational skills
  • Strong interpersonal communication skills
  • Strong technical writing and written communication skills
  • Working knowledge of Windows based office productivity tools including word processor and spreadsheet

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