ZipRecruiter

Log In

1

Clinical Science Manager Jobs (NOW HIRING)

Bayer Inc.

Director, Clinical Science Lead

Cambridge, MA

$169K - $254K/yr

... management, evaluation, and documentation; * Promotes a creative and innovation-friendly collaboration between clinicians and scientists to evolve Early Clinical Development Oncology's unique value ...

Travere

Director, Clinical Science

San Diego, CA · On-site +1

$84K - $115K/yr

The Director, Clinical Science, will provide management and support for Travere's on-going and future nephrology development and life-cycle activities for clinical programs. The position will work ...

Bayer

Director, Clinical Science Lead

Cambridge, MA · On-site

$169K - $254K/yr

... management, evaluation, and documentation; * Promotes a creative and innovation-friendly collaboration between clinicians and scientists to evolve Early Clinical Development Oncology's unique value ...

Olema Oncology

Director, Clinical Science

San Francisco, CA · On-site

$94K - $128K/yr

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

Travere Therapeutics

Director, Clinical Science

San Diego, CA · On-site

$86K - $117K/yr

The Director, Clinical Science, will provide management and support for Travere's on-going and future nephrology development and life-cycle activities for clinical programs. The position will work ...

Bayer

Director, Clinical Science Lead

Cambridge, MA · On-site

$169K - $254K/yr

... management, evaluation, and documentation; Promotes a creative and innovation-friendly collaboration between clinicians and scientists to evolve Early Clinical Development Oncology's unique value ...

Natera

Associate Director, Clinical Science

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

Director, Clinical Science Lead

Boston, MA

$169K - $254K/yr

... management, evaluation, and documentation; Promotes a creative and innovation-friendly collaboration between clinicians and scientists to evolve Early Clinical Development Oncology's unique value ...

Natera

OR · On-site

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 ...

IQVIA

Director, Clinical Science, Cronos

Bethlehem, PA

$79K - $107K/yr

Ensure Clinical Team escalations are managed appropriately and in consultation with other ... Clinical Science, as required. * Perform data preparation activities-including cleaning ...

next page

Showing results 1-20

All JobsClinical Science Manager Jobs

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:
What states have the most Clinical Science Manager jobs? States with the most job openings for Clinical Science Manager jobs include:
What job categories do people searching Clinical Science Manager jobs look for? The top searched job categories for Clinical Science Manager jobs are:
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.
Director, Clinical Science

Director, Clinical Science

Monte Rosa Therapeutics, Inc

Boston, MA • On-site

$185K - $240K/yr

Full-time

Posted 14 days ago

Job description

Overview
The Director Clinical Scientist is an important and visible member of the Clinical Development team, working collaboratively with the Clinical operations lead and medical director. The Director Clinical Scientist will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Early- stage portfolio. The role is the primary contact for internal and external stakeholders for clinical aspects of the protocol, supporting strategic development, providing final recommendations to senior management.
Responsibilities
  • Supports the clinical lead or in some instances serve as clinical lead of early phase program(s)
  • Independently leads clinical execution of one or more studies. May be accountable for program level clinical deliverables.
  • Leads development of the protocol, and associated amendment(s) ensuring high level of quality, and operational delivery. Partners with or support from Clinical Lead in governance review and approval process. Leads development, review or approval of key documents such as the Informed Consent Documents (ICD), Investigator Brochure, Investigators Letters, and safety documents.
  • Leads the development of recommendations on strategies to internal committees
  • Provides scientific/medical guidance to the study team, including the CRO team
  • Reviews safety data, serious adverse events (SAE) reports, and authors or reviews safety or regulatory documents and updates them as required. Tracks SAE and leads presentation of data during Safety Review Team meetings.
  • Collaborates with research scientists and translational scientists to provide clinical input in crafting and evaluating data to support development of pre-clinical compound(s)
  • Leads the development and review of content and quality of publications and inputs to development of the publication strategy
  • Leads the examination and interpretation of clinical data at the study and program level. Author or reviews the Clinical Study Report including the review of narratives.
  • Attends (in person or by TC) the Site Initiation Visits, to present the study design and key aspects of the protocol
  • Leads the compilation and analysis of the data for and from the dose critical issue committee/safety review committee, in collaboration with the program physician
  • Develops, builds and maintains investigator and site relationships to support site selection and study start up activities
  • Represents the project internally and supports drug development externally as a medical scientific expert with key external experts. Supports development of alliances as appropriate.

Qualifications
  • Ph.D., PharmD or a Masters degree in a relevant Clinical or Biomedical field.
  • 8 plus years of clinical drug development or medical research experience within a pharmaceutical/biotech or academic environment
  • Oncology or immunology experience
  • Advanced understanding of clinical practice across tumor types and how clinical practice is evolving with the introduction of new therapies. Understanding of cancer cell biology.
  • Experience leading delivery and influencing at senior leadership levels both internally and externally
  • Experience in working and leading in matrix teams
  • Strong collaborative communications skills including the ability to engage with a diverse internal and external client base and lead through conflict
  • Proven ability in problem solving and issues management that is solution focused
  • Experience in collaborating externally in terms of clear requirements for collaborative contracts, influencing delivery and scientific engagement.
  • Effective communication, presentation and organizational skills to ensure coordinated and timely delivery of projects
  • Demonstrated scientific writing skills
  • Embraces Artificial Intelligence and other evolving technologies and adopts best practices aimed at improving efficiency and quality of clinical practice
  • Proven team leadership experience in a clinical setting (2-3 years)
  • Ability to work proactively and independently, organizational skills, prioritizes self and others.
  • Ability to support and mentor junior team members

Apply