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Clinical Science Manager Jobs in Boston, MA (NOW HIRING)

Relay Therapeutics

Manager, Clinical Science

Cambridge, MA · On-site

$71K - $97K/yr

As Manager, Clinical Science at Relay Tx, you will play a key role in driving the development of our assets and support the implementation and execution of the clinical strategy. You will work ...

Olema Oncology

Director, Clinical Science

Boston, MA · On-site

$220K - $250K/yr

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

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:

eGenesis

Associate Director, Clinical Science

Cambridge, MA · On-site

$175 - $226/hr

The Associate Director, Clinical Science is responsible for the planning, execution and operational ... Lead data review, evaluation, and analyses in collaboration with Data Management and Biostatistics ...

BioNTech SE

Director, Clinical Science

Cambridge, MA · On-site

$168K - $268K/yr

As Director, Clinical Science (m/f/d), you will lead and shape clinical development strategies ... manage adverse event * Drive the creation of key study-level documents such as protocols ...

eGenesis

Associate Director, Clinical Science

Cambridge, MA · On-site

$175K - $226K/yr

Lead data review, evaluation, and analyses in collaboration with Data Management and Biostatistics ... PharmD or PhD with 7+ years of clinical science experience in a biotech or pharmaceutical company ...

BioNTech SE

Director, Clinical Science

Cambridge, MA

$168K - $268K/yr

As Director, Clinical Science (m/f/d), you will lead and shape clinical development strategies ... manage adverse event * Drive the creation of key study-level documents such as protocols ...

TScan Therapeutics

Clinical Scientist

Waltham, MA

Experience * 5-8+ years of experience in clinical development, clinical science, data management, or related functions within biotechnology, pharmaceutical, or CRO environments. * Demonstrated ...

TScan Therapeutics

Clinical Scientist

Waltham, MA · On-site

Experience * 5 8+ years of experience in clinical development, clinical science, data management, or related functions within biotechnology, pharmaceutical, or CRO environments. * Demonstrated ...

TScan Therapeutics

Clinical Scientist

Waltham, MA

Experience * 58+ years of experience in clinical development, clinical science, data management, or related functions within biotechnology, pharmaceutical, or CRO environments. * Demonstrated ...

Clinovo

Sr Clinical Scientist

Cambridge, MA · On-site

The successful candidate will bring strong clinical science expertise and experience supporting ... Safety & Risk Management * Collaborate closely with Pharmacovigilance, Medical Safety, and Medical ...

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All JobsClinical Science JobsClinical Science Manager JobsClinical Science Manager Jobs in Boston, MA

Clinical Science Manager information

See Boston, MA salary details

$47.3K

$89.5K

$152.1K

How much do clinical science manager jobs pay per year?

As of Aug 30, 2026, the average yearly pay for clinical science manager in Boston, MA is $89,466.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,600.00 and $97,200.00 per year, depending on experience, location, and employer.

What is a clinical science manager?

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 are the key skills and qualifications needed to thrive as a clinical science manager?

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.

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 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 popular job titles related to Clinical Science Manager jobs in Boston, MA?

For Clinical Science Manager jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Clinical Science Manager jobs in Boston, MA look for?

The top searched job categories for Clinical Science Manager jobs in Boston, MA are:

What cities near Boston, MA are hiring for Clinical Science Manager jobs?

Cities near Boston, MA with the most Clinical Science Manager job openings:

Clinical Science Manager jobs near you
Infographic showing various Clinical Science Manager job openings in Boston, MA as of July 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $89,466 per year, or $43 per hour.

Manager, Clinical Science

Relay Therapeutics

Cambridge, MA • On-site

$71K - $97K/yr

Full-time

Posted 16 days ago

Job description

The Opportunity:
As Manager, Clinical Science at Relay Tx, you will play a key role in driving the development of our assets and support the implementation and execution of the clinical strategy. You will work closely with clinical project management, regulatory affairs, clinical operations, biostatistics, data management, and medical writing to advance one or more clinical studies. You will have the opportunity to make an impact through providing your strategic and scientific input to cross functional teams.
Your Role:
  • Contribute to the design of clinical studies in close collaboration with the Medical Lead as well as Clinical Development team.
  • Lead and/or contribute to protocol development with medical writing by translating the approved protocol concept into executable/efficient clinical protocols
  • Drive the medical contribution together with Medical Leads to annual update of IB, DSUR liaising with cross functional teams
  • Support Medical Leads to answer regulatory queries and contribute to other submissions related to studies
  • Perform medical data review and analysis of study results; and review protocol deviations to identify cause and appropriate resolution.
  • Contribute to the design of electronic case report forms, ensuring that eCRFs accurately capture the data intended to be gathered per protocol.
  • Support data cleaning activities requiring medical interpretation and analyses of data for regulatory submissions, data disclosure and scientific publications
  • Support Medical Lead to monitor real time study data to ensure the integrity of the study and the study data and working closely with clinical operations team to answer protocol related questions and resolve any study conduct issues from investigative sites
  • Review and summarize relevant literature for competitive intelligence, and author and review manuscripts, abstracts, posters, etc.
  • Managing communication and building strong collaborative relationships with key stakeholders both internally and externally, including interactions with academic experts, clinical trial investigators, and other clinical stakeholders.

Your Background:
  • Advanced degree in life sciences: PhD and/or MS, PharmD, BSN in relevant scientific field; with 2 years of experience in pharmaceutical and/or biotech industry.
  • Knowledge of the clinical development process with the ability to understand concepts of various phases and principles of study design is required
  • Thorough understanding of ICH, GCP, and relevant regulatory requirements is required
  • Experience in early/ late phase development and oncology preferred
  • Strong interpersonal, organization, planning and communication and writing skills.
  • Ability to prioritize and manage multiple tasks simultaneously, being a team player, being flexible and have hands-on attitude.
  • Ability to influence with collaboration, and drive decision-making within multi-disciplinary teams

#JO1
About Relay Therapeutics
Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.
Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you're excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us!

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