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Masters Of Clinical Science Jobs (NOW HIRING)

SystImmune, Inc

Director of Clinical Science

Princeton, NJ · On-site

$180K - $250K/yr

... degree such as a Masters, PharmD, PhD in biological/pharmaceutical science, or MD. * Minimum ... well as clinical research. * Therapeutic areas of expertise must include oncology. * Advanced ...

Systimmune

Director of Clinical Science

Princeton, NJ · On-site

$180K - $250K/yr

... degree such as a Masters, PharmD, PhD in biological/pharmaceutical science, or MD. * Minimum ... well as clinical research. * Therapeutic areas of expertise must include oncology. * Advanced ...

MSD

Senior Director of Clinical Science - Lung

Rahway, NJ · On-site

$81K - $110K/yr

Reporting to the Executive Director - Lung, Head and Neck, and Gastrointestinal, or to the Head of Clinical Science Oncology, this role contributes to disease area strategy by applying deep ...

Merck & Co.

$86K - $118K/yr

Reporting to the Executive Director - Lung, Head and Neck, and Gastrointestinal, or to the Head of Clinical Science Oncology, this role contributes to disease area strategy by applying deep ...

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Masters Of Clinical Science information

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How much do masters of clinical science jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for masters of clinical science in the United States is $34.62, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $32.93 per hour, depending on experience, location, and employer.

What is the difference between Masters Of Clinical Science vs Clinical Research Coordinator?

AspectMasters Of Clinical ScienceClinical Research Coordinator
Required CredentialsMaster's degree in clinical science or related fieldBachelor's degree often required; some roles prefer certification
Work EnvironmentResearch institutions, hospitals, academiaClinical trial sites, hospitals, research organizations
Employer & Industry UsageUniversities, research institutes, pharmaceutical companiesClinical trial sites, CROs, hospitals
Common Search & Comparison IntentUnderstanding advanced research roles, qualificationsJob responsibilities, certifications, career path

The Masters Of Clinical Science typically involves advanced research training and a master's degree, preparing individuals for research-focused roles in academia or industry. Clinical Research Coordinators usually hold a bachelor's degree and focus on managing clinical trials at research sites. While both roles work within clinical research, the Masters Of Clinical Science is more research and academically oriented, whereas Clinical Research Coordinators handle trial logistics and participant management.

What can I do with a Masters of Clinical Science degree?

A Masters of Clinical Science prepares graduates for roles in clinical research, healthcare settings, and medical device development. Graduates often work as clinical research coordinators, medical science liaisons, or in regulatory affairs, utilizing skills in data analysis, patient interaction, and medical protocols.

What can you do with a Masters of Clinical Science?

A Masters of Clinical Science prepares graduates for roles in clinical research, healthcare settings, and medical device development. Common positions include clinical research coordinator, medical science liaison, and clinical trial manager, often requiring knowledge of regulatory standards and data analysis tools.

What are popular job titles related to Masters Of Clinical Science jobs?

For Masters Of Clinical Science jobs, the most frequently searched job titles are:

Infographic showing various Masters Of Clinical Science job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 16% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $72,002 per year, or $34.6 per hour.

Director of Clinical Science

Princeton, NJ • On-site

SystImmune, Inc
Biotechnology Research and Development • 1 - 10 employees
Learn more about SystImmune, Incexternal

$180K - $250K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 8 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
Responsibilities:
  • Contributes to developing the program strategy for assigned trials/compounds.
  • Author components with the Medical Director and reviewer of clinical and regulatory documents and registration dossiers (i.e., protocol, ICF, IB, safety updates, study reports, regulatory submissions, etc.) to support registration and commercialization of the compound(s).
  • Contributes to the development of eCRFs and eCRFs completion guidelines and provides scientific support for other key data management deliverables (e.g., database lock activities).
  • Lead the development of a medical data review plan, medical monitoring plan, perform ongoing medical data review, and summarize efficacy and safety data for interpretation/analysis.
  • Provide input for country/site selection and feasibility assessment and interact with KOLs.
  • Prepare charters and coordinate internal/external committee meetings including presentations and discussion with senior leadership.
  • Participate in the development and review of study plans and liaise with project teams.
  • Prepare presentations for Investigator meetings, site personnel, CRA training, pre-study site visits (SEVs), and site initiation visits (SIVs).
  • Provide input for developing publications in coordination with the Scientific Communications/Publishing department.
Qualifications:
  • Bachelor's degree in life sciences or health-related field with an advanced degree such as a Masters, PharmD, PhD in biological/pharmaceutical science, or MD.
  • Minimum requirement: at least 8 or more years industry experience including pre-clinical as well as clinical research.
  • Therapeutic areas of expertise must include oncology.
  • Advanced knowledge and skills to support program-specific data review, trend identification, data interpretation.
  • Knowledge of the International Council of Harmonization (ICH), GCP, and other relevant regulatory guidelines.
  • Advanced ability to analyze clinical information succinctly and efficiently with strong written communication.
  • Outstanding track record of strong communication, presentation, analytic, and strategic capabilities and ability to effectively collaborate with medical experts.

Compensation and Benefits:
The expected base salary range for this position is $180,000 to $230,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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