... Associate Director, RWE Operations) leads the operational execution of a U.S.-based real-world ... Serve as the primary study lead responsible for end-to-end study management, including planning ...
New
Quick apply
... Associate Director, RWE Operations) leads the operational execution of a U.S.-based real-world ... Serve as the primary study lead responsible for end-to-end study management, including planning ...
New
Quick apply
... Associate Director, RWE Operations) leads the operational execution of a U.S.-based real-world ... Serve as the primary study lead responsible for end-to-end study management, including planning ...
New
The Opportunity The Associate Director, Clinical Compliance & Records will work closely and ... Provide Study Management Teams (SMTs) with guidance on the application of ICH-GCP standards, FDA ...
New
The Opportunity The Associate Director, Clinical Compliance & Records will work closely and ... Provide Study Management Teams (SMTs) with guidance on the application of ICH-GCP standards, FDA ...
New
The Opportunity The Associate Director, Clinical Compliance & Records will work closely and ... Provide Study Management Teams (SMTs) with guidance on the application of ICH-GCP standards, FDA ...
New
The Opportunity The Associate Director, Clinical Compliance & Records will work closely and ... Provide Study Management Teams (SMTs) with guidance on the application of ICH-GCP standards, FDA ...
New
Responsible for day-to-day management of vendors working on assigned study, including setting ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Responsible for day-to-day management of vendors working on assigned study, including setting ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Cambridge, MA · On-site
Management of the study budget, including Task Orders, Change Orders, invoice approval and ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Cambridge, MA · On-site
Management of the study budget, including Task Orders, Change Orders, invoice approval and ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Management of the study budget, including Task Orders, Change Orders, invoice approval and ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Management of the study budget, including Task Orders, Change Orders, invoice approval and ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Overview Alnylam is seeking a highly collaborative Associate Director, Clinical Portfolio ... Partner with the Senior Director and stakeholders across Clinical Operations, Study Management ...
Overview Alnylam is seeking a highly collaborative Associate Director, Clinical Portfolio ... Partner with the Senior Director and stakeholders across Clinical Operations, Study Management ...
Boston, MA · Hybrid
$125K/yr
This position is responsible for managing studies across solid organ platforms. The Senior Clinical Research Associate will report to the VP Scientific and Medical Affairs and will play an important ...
Boston, MA · Hybrid
$125K/yr
This position is responsible for managing studies across solid organ platforms. The Senior Clinical Research Associate will report to the VP Scientific and Medical Affairs and will play an important ...
Lexington, MA · On-site
$48K - $60K/yr
Medicilon USA is seeking a Research Associate II to support the execution of preclinical in vivo ... study conduct and promptly communicate concerns to study management and veterinary staff.
Quick apply
Lexington, MA · On-site
$48K - $60K/yr
Medicilon USA is seeking a Research Associate II to support the execution of preclinical in vivo ... study conduct and promptly communicate concerns to study management and veterinary staff.
Boston, MA · On-site
$125K/yr
This position is responsible for managing studies across solid organ platforms. The Senior Clinical Research Associate will report to the VP Scientific and Medical Affairs and will play an important ...
Boston, MA · On-site
$125K/yr
This position is responsible for managing studies across solid organ platforms. The Senior Clinical Research Associate will report to the VP Scientific and Medical Affairs and will play an important ...
$48K - $60K/yr
Medicilon USA is seeking a Research Associate II to support the execution of preclinical in vivo ... study conduct and promptly communicate concerns to study management and veterinary staff.
Quick apply
$48K - $60K/yr
Medicilon USA is seeking a Research Associate II to support the execution of preclinical in vivo ... study conduct and promptly communicate concerns to study management and veterinary staff.
Lexington, MA · On-site
$48K - $60K/yr
Medicilon USA is seeking a Research Associate II to support the execution of preclinical in vivo ... study conduct and promptly communicate concerns to study management and veterinary staff.
Quick apply
Lexington, MA · On-site
$48K - $60K/yr
Medicilon USA is seeking a Research Associate II to support the execution of preclinical in vivo ... study conduct and promptly communicate concerns to study management and veterinary staff.
... study management tools. Coordinates and drives operational strategies within the assigned projects ... associates from different countries, disciplines and levels. * A strong customer focus along with ...
... study management tools. Coordinates and drives operational strategies within the assigned projects ... associates from different countries, disciplines and levels. * A strong customer focus along with ...
Cambridge, MA · On-site
Responsible for day-to-day management of vendors working on assigned study, including setting ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Cambridge, MA · On-site
Responsible for day-to-day management of vendors working on assigned study, including setting ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
The Data Management (DM) Quality Associate will ... Review study documentation ensuring data quality is consistent with DM best practices, standards ...
The Data Management (DM) Quality Associate will ... Review study documentation ensuring data quality is consistent with DM best practices, standards ...
... study management tools. Coordinates and drives operational strategies within the assigned projects ... associates from different countries, disciplines and levels. * A strong customer focus along with ...
... study management tools. Coordinates and drives operational strategies within the assigned projects ... associates from different countries, disciplines and levels. * A strong customer focus along with ...
Cambridge, MA · On-site
Responsible for day-to-day management of vendors working on assigned study, including setting ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Cambridge, MA · On-site
Responsible for day-to-day management of vendors working on assigned study, including setting ... Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation ...
Boston, MA · On-site
$82K - $124K/yr
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 ...
Boston, MA · On-site
$82K - $124K/yr
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 ...
Boston, MA · On-site
$82K - $124K/yr
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 ...
Boston, MA · On-site
$82K - $124K/yr
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 ...
Boston, MA · On-site
$82K - $124K/yr
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 ...
Boston, MA · On-site
$82K - $124K/yr
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 ...
$11.32 - $15.95
4% of jobs
$15.95 - $20.59
9% of jobs
$20.59 - $25.22
9% of jobs
$28.46 is the 25th percentile. Wages below this are outliers.
$25.22 - $29.85
5% of jobs
$29.85 - $34.48
4% of jobs
$34.48 - $39.11
4% of jobs
$39.11 - $43.75
10% of jobs
The median wage is $45.40 / hr.
$43.75 - $48.38
15% of jobs
$48.38 - $53.01
12% of jobs
$54.48 is the 75th percentile. Wages above this are outliers.
$53.01 - $57.64
12% of jobs
$57.64 - $62.27
17% of jobs
$11
$43
$62
| Aspect | Study Management Associate | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, relevant certifications often preferred | Bachelor's degree, often with certifications like CCRP |
| Work Environment | Pharmaceutical companies, CROs, research institutions | Hospitals, clinics, research sites |
| Employer & Industry Usage | Used in industry-sponsored trials and clinical research firms | Common in academic and hospital-based studies |
| Search & Comparison Intent | High overlap in job duties and qualifications | Similar 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.
Contractor
Medical, Dental, Vision, Life, Retirement, PTO
Posted 13 hours ago
The Senior Manager, Medical Affairs Lead (Senior Manager/Associate Director, RWE Operations) leads the operational execution of a U.S.-based real-world evidence study within the Medical Affairs organization. This role serves as the primary study lead, overseeing CRO partners, driving study startup activities, managing timelines and risks, and guiding cross-functional teams to deliver high-quality post-approval and observational research that supports medical and commercial objectives.
Responsibilities
This role is based in a hybrid work environment in Waltham, MA, with an expectation to work on-site three days per week. The setting combines in-office collaboration with remote flexibility, supporting close interaction with cross-functional teams in Medical Affairs and related functions. The organization focuses on discovering and advancing innovative, life-transforming therapeutics for people living with genetically driven neuromuscular diseases, leveraging a platform designed to deliver targeted therapeutics to muscle and the central nervous system. The culture emphasizes scientific innovation, patient-centered impact, and cross-functional partnership across a broad pipeline that includes clinical and preclinical programs in neuromuscular and rare diseases.
Job Type & Location
This is a Contract position based out of Waltham, MA.
Pay and BenefitsThe pay range for this position is $90.00 - $120.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
This is a hybrid position in Waltham,MA.
Application DeadlineThis position is anticipated to close on Jul 10, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
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Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
5,001 - 10,000 Employees
Hanover, MD, US
1983