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Study Management Associate Jobs in Boston, MA (NOW HIRING)

RadNet

Senior Clinical Studies Associate

Somerville, MA · On-site

$71K/yr

Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Working under the guidance of Clinical Study Manager and cross-functional study teams, the SCSA ...

Deephealth

Senior Clinical Studies Associate

Somerville, MA · On-site

$71K - $96K/yr

Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Working under the guidance of Clinical Study Manager and cross-functional study teams, the SCSA ...

RadNet

Senior Clinical Studies Associate

Somerville, MA

$71K - $96K/yr

Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Working under the guidance of Clinical Study Manager and cross-functional study teams, the SCSA ...

RadNet

Senior Clinical Studies Associate

Somerville, MA

$71K - $96K/yr

Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Working under the guidance of Clinical Study Manager and cross-functional study teams, the SCSA ...

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All JobsStudy Management Associate JobsStudy Management Associate Jobs in Boston, MA

Study Management Associate information

See Boston, MA salary details

$11

$43

$62

How much do study management associate jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for study management associate in Boston, MA is $43.21, according to ZipRecruiter salary data. Most workers in this role earn between $28.56 and $56.36 per hour, depending on experience, location, and employer.

What is a study management associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.

What are the typical responsibilities of a study management associate?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

What are the key skills and qualifications needed to thrive as a study management associate?

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What is the difference between Study Management Associate vs Clinical Research Coordinator?

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What are popular job titles related to Study Management Associate jobs in Boston, MA?

For Study Management Associate jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Study Management Associate jobs in Boston, MA look for?

The top searched job categories for Study Management Associate jobs in Boston, MA are:

Study Management Associate jobs near you
Infographic showing various Study Management Associate job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $89,870 per year, or $43.2 per hour.

Research Associate II In Vivo Pharmacology

MEDICILON USA CORP

Lexington, MA • On-site

$48K - $60K/yr

Full-time

Re-posted 16 days ago

Job description

Medicilon USA is seeking a Research Associate II to support the execution of preclinical in vivo pharmacology and disease model studies. The successful candidate will have hands-on experience conducting rodent studies in a CRO, biotechnology, or pharmaceutical environment and will be responsible for study execution, animal procedures, sample collection, and data documentation.
This position works closely with study scientists and project teams to ensure high-quality study conduct, adherence to timelines, and compliance with animal welfare and regulatory requirements.
Key Responsibilities
  • Perform routine animal handling, restraint, dosing, monitoring, and sample collection activities in rodent models.
  • Prepare test article formulations and perform dose calculations according to study protocols.
  • Administer compounds through common routes including oral gavage, intravenous (IV), subcutaneous (SC), and intraperitoneal (IP) administration.
  • Conduct blood collection, tissue collection, necropsy, and other study-related procedures.
  • Perform protocol-specific assessments, including body weight collection, clinical observations, disease scoring, and other in-life measurements.
  • Support study initiation activities, including preparation of study materials, labeling, room setup, and protocol review.
  • Accurately record procedures, observations, and study data in laboratory notebooks, electronic systems, and study records.
  • Ensure studies are conducted in accordance with approved protocols, IACUC requirements, SOPs, and company policies.
  • Monitor animal health and welfare throughout study conduct and promptly communicate concerns to study management and veterinary staff.
  • Maintain laboratory equipment, supplies, and inventory required for study execution.
  • Collaborate effectively with scientists and cross-functional teams to support project timelines and deliverables.
  • Participate in training activities and continuously develop technical skills and knowledge.
  • Perform all activities in compliance with applicable regulations, company policies, and training requirements.
  • Other duties and responsibilities as assigned.
Qualifications
Required:
  • Bachelor's degree in Biology, Animal Science, Life Sciences, or a related scientific discipline. 
  • 1–3 years of hands-on in vivo experience in a CRO, biotechnology, pharmaceutical, or related industry environment.
  •  Experience with rodent handling, restraint, dosing, and animal monitoring. 
  •  Experience administering compounds through common routes including oral gavage, intravenous (IV), subcutaneous (SC), and intraperitoneal (IP) injection. 
  •  Experience with blood collection, tissue collection, necropsy, and sample processing. 
  •  Experience executing studies according to protocols, SOPs, and regulatory requirements. 
  •  Familiarity with IACUC requirements and animal welfare regulations. 
  •  Experience supporting pharmacology, efficacy, or disease model studies. 
  •  Strong attention to detail and ability to maintain accurate study documentation. 
  •  Ability to manage multiple priorities and work effectively in a fast-paced team environment. 
  •  Strong communication and organizational skills. 
Preferred:
  •  ALAT certification or equivalent laboratory animal training. 
  •  Experience working in a GLP-regulated environment. 
  •  Experience with immunology, inflammation, metabolic disease, or other therapeutic areas. 
  •  Experience with additional in vivo techniques such as PK sampling, telemetry, surgical support, or specialized model assessments.