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Study Management Associate Jobs in Massachusetts

RadNet

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 ...

Deephealth

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 ...

Apply Early

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 ...

Apply Early

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 ...

Prometrika LLC

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

... Trial Associates (CTA) and other study staff, as needed * Recommend and implement innovative process ideas to impact clinical trials management * Organize and manage internal team meetings ...

Novartis

Manager, Operations

Cambridge, MA · Hybrid

$103K - $192K/yr

... study management tools. Coordinates within the assigned projects and acts as the interface between ... associates from different countries, disciplines and levels. * A strong customer focus along with ...

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All JobsStudy Management Associate JobsStudy Management Associate Jobs in Massachusetts

Study Management Associate information

See Massachusetts salary details

$11

$43

$62

How much do study management associate jobs pay per hour?

As of Jul 3, 2026, the average hourly pay for study management associate in Massachusetts is $43.30, according to ZipRecruiter salary data. Most workers in this role earn between $28.62 and $56.48 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Study Management Associate, and why are they important?

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 the typical responsibilities of a Study Management Associate in a clinical research team?

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 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 popular job titles related to Study Management Associate jobs in Massachusetts? For Study Management Associate jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Study Management Associate jobs in Massachusetts look for? The top searched job categories for Study Management Associate jobs in Massachusetts are:
What cities in Massachusetts are hiring for Study Management Associate jobs? Cities in Massachusetts with the most Study Management Associate job openings:
Study Management Associate jobs near you
Senior Clinical Study Administrator

Senior Clinical Study Administrator

AstraZeneca

Boston, MA • On-site

$82K - $124K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

16th of 73 rated pharmaceutical

Job description

This is what you will do:
The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time, cost and quality objectives according to Good Clinical Practices (GCP), Alexion Standard Operating Procedures (SOPs) and evolving regulatory requirements.
The CSA collaborates closely with the Project Manager Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country.
You will be responsible for:
  • Providing support to the local study team in COM in achieving quality and timeliness of study deliverables across the lifecycle of assigned trials (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation)
  • End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the Clinical Trial Management System (CTMS) and other general trial support in the country or region as delegated or per assigned trials.
  • Providing support to the local study team including for start up activities in start-up phase: CDA delivery and negotiation, distribution and collection of documents, communication with sites during contract negotiation phase, Site File preparation and preparation and approval of sites for activation, etc
  • Collaborating with PMCO, CRAs, SSU manager and study vendors on the preparation, supports the handling and distribution of clinical trial supplies and maintenance of tracking information
  • Act as a central point of contact for the local study team in COM for designated project communications, correspondence, and associated documentation.
  • Input on the development and maintenance of project management and other global tracking tools (e.g: CTMS, smartsheets, etc).
  • Collaborating in global initiatives to standardize processes within and across countries (collaboration with other local and global CSAs)
  • Assist with local language translations, IRB/CEC/CA submissions in collaboration with Regulatory Affairs and other functions, as required within the country/region.
  • Providing support to local COM team with local F2F study and team meetings (venue, cost, agenda, etc), support team teleconferences, assist with staff onboarding as required by country/region
  • Depending on the country/region, the CSA may provide varying levels of COM support to the department rather than to assigned studies as needed.

You will need to have:
  • Bachelor's Degree in a related discipline, preferably life science.
  • Proficiency with MS Office Suite (excel, word, PowerPoint)
  • Understanding of the drug development process either via education or experience in the life sciences field.
  • Preferably minimum experience of 3 year in Development
  • Excellent collaboration and interpersonal skills, unafraid to ask questions.
  • Strong organizational skills and ability to manage competing priorities.
  • Strong attention to detail
  • Effective written and verbal communication skills

We would prefer for you to have:
  • Prior experience working in clinical research
  • Medical knowledge and ability to learn relevant Alexion rare disease areas.
  • Ability to work in an environment of remote collaborators and in a matrix reporting structure
  • Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.
  • Ability to look for and champion more efficient and effective methods/ processes of delivering quality clinical trials with reduced budget and in less time.
  • Team oriented and flexible; ability to respond quicky to shifting demands and opportunities
  • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.

The annual base pay (or hourly rate of compensation) for this position ranges from $82,798 to $124,196. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
23-Jun-2026
Closing Date
06-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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