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Study Director Jobs in Massachusetts (NOW HIRING)

Kymera Therapeutics

Director, Study Start-Up

Watertown, MA · On-site

$195K - $275K/yr

... study start-up activities, partnering with Quality Assurance as needed. Skills and experience you'll bring: * 10+ years of experience in the biotech/pharmaceutical industry with direct experience in ...

Alkermes

Director, Clinical Pharmacology

Waltham, MA · On-site

$228K - $246K/yr

... study design and execution. This role requires the person to be onsite 3x a week in our Waltham, MA ... Direct experience with pharmacokinetic/pharmacodynamic modeling, bioanalytical analysis, and non ...

Alkermes

Director, Clinical Pharmacology

Waltham, MA · On-site

$228K - $246K/yr

Contributing to clinical program design, trial protocols, analysis plans, study reports and ... Direct experience with pharmacokinetic/pharmacodynamic modeling, bioanalytical analysis, and non ...

Vrtx

Senior Director, Clinical Pharmacology

Boston, MA · Hybrid

$232K - $348K/yr

Manages a group of Clinical Pharmacologists at Director-level and below to set strategy, develop and execute Clinical Pharmacology plans and studies for Disease Area programs * Directs Clinical ...

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Study Director information

See Massachusetts salary details

$49.1K

$140.2K

$253.9K

How much do study director jobs pay per year?

As of Aug 21, 2026, the average yearly pay for study director in Massachusetts is $140,193.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,300.00 and $205,900.00 per year, depending on experience, location, and employer.

What is a study director?

A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.

What does a study director do?

As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

How does a study director typically collaborate with cross-functional teams during a research project?

As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.

What skills and qualifications does a successful study director have?

To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.

What is the difference between Study Director vs Laboratory Manager?

AspectStudy DirectorLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and relevant certificationsRequires relevant degrees and management experience, but not necessarily advanced research credentials
Work EnvironmentLeads specific research or regulatory studies, often in contract labs or pharmaceutical companiesOversees daily lab operations, staff, and compliance across multiple projects
Industry UsageCommonly used in GLP, clinical, and research settingsUsed broadly in laboratory settings across industries

The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.

More about Study Director jobs

What are the most commonly searched types of Study jobs in Massachusetts?

The most popular types of Study jobs in Massachusetts are:

What are popular job titles related to Study Director jobs in Massachusetts?

For Study Director jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Study Director jobs in Massachusetts look for?

The top searched job categories for Study Director jobs in Massachusetts are:

What cities in Massachusetts are hiring for Study Director jobs?

Cities in Massachusetts with the most Study Director job openings:

Study Director jobs near you
Infographic showing various Study Director job openings in Massachusetts as of August 2026, with employment types broken down into 76% Full Time, 20% Part Time, 2% Temporary, and 2% Contract. Highlights an 94% In-person, 2% Hybrid, and 4% Remote job distribution, with an average salary of $140,193 per year, or $67.4 per hour.

Director, Study Start-Up

Kymera Therapeutics

Watertown, MA

$195K - $275K/yr

Full-time

Re-posted 7 days ago

Job description

Who we are:

Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visitwww.kymeratx.com or follow us onX (formerly Twitter)orLinkedIn. 

How we work:
  • PIONEER: We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines.
  • COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.
  • BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.
How you'll contribute:
  • Provide strategic and operational leadership for endtoend study startup activities across assigned clinical programs, ensuring timely, compliant, and highquality site activation.
  • Accountable for development, execution, and ongoing optimization of studyspecific startup strategies, including country selection, regulatory and ethics submissions, site feasibility and selection, contract and budget execution, and site activation readiness.
  • Establish and maintain clear startup timelines, metrics, and dashboards; proactively identify risks to activation timelines and drive mitigation plans to achieve firstpatientin (FPI) and enrollment targets.
  • Provide oversight of country and sitelevel regulatory and ethics submissions (e.g., IRB/EC/HA), ensuring consistency with global strategy and local regulatory requirements.
  • Ensure quality, completeness, and inspection readiness of startup documentation, including Trial Master File (TMF) content and countrylevel startup records, in accordance with GCP and internal SOPs.
  • Partner with Clinical Research Organization(s) to oversee site contract and budget negotiations, ensuring alignment with approved study budgets and timely execution to support activation timelines.
  • Serve as the primary escalation point for complex startup challenges, including site readiness or performance risks, regulatory delays or vendor issues; communicate status and resolution plans to senior leadership.
  • Contribute to portfoliolevel planning by providing startup insights and recommendations to inform study design, country strategy, resourcing, and feasibility assumptions.
  • Develop and maintain study startup processes, systems, and tools to reduce cycle times, improve quality, and enhance predictability of startup delivery.
  • Ensure startup activities are conducted in compliance with global regulations, internal policies, and company quality standards, maintaining a strong focus on patient safety and data integrity.
  • Support organizational readiness for audits and inspections related to study startup activities, partnering with Quality Assurance as needed.
Skills and experience you'll bring:
  • 10+ years of experience in the biotech/pharmaceutical industry with direct experience in project management within Clinical Operations
  • Proven track record in process improvement, clinical trial execution, and operational strategy.
  • Experience with planning, management, and oversight of activities and deliverables within Clinical Operations
  • Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance
  • Proven track record of managing multiple projects and/or programs concurrently
  • Excellent analytical, problem-solving, and organizational skills.
  • Strong communication and interpersonal skills with the ability to influence cross-functional stakeholders.
  • Demonstrated ability to lead change and foster a culture of continuous improvement.

 

Equal Employment Opportunity

Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.  All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.

Compensation

  • Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.
  • The anticipated base salary range for this role is $195,000 - $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.
  • Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate's depth of experience and the capabilities they bring to the position.

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