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Associate Clinical Data Manager Jobs (NOW HIRING)

Clinical Data Manager

Waltham, MA ยท On-site

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

Provide clinical data management support for study operations and analysis groups including the following. o Assist in defining and creation of data listings, including programming software to ...

Clinical Data Manager

Redmond, WA ยท On-site

$100K - $170K/yr

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data ...

ZS is seeking a Tech Project Delivery Manager to lead a high-velocity team focused on the future of Biometrics and Clinical Data. We are looking for a delivery leader who excels at navigating the ...

Clinical Data Manager

Redmond, WA ยท On-site

$100K - $170K/yr

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data ...

Agile Decision Sciences LLC is looking for a Clinical Data Manager to support the growing team. Responsibilities : * Manage the delivery of high-quality data from project start-up and planning to ...

Clinical Data Manager

Menlo Park, CA ยท On-site

$42 - $50/hr

Enter and update study data using the Clinical Trial Management System. * Provide training and guidance to lower-level coordinators. * Participate in the interview and selection process of new ...

Experience managing a team * Familiarity with clinical research protocols and manuscripts ... Ability to handle and interact with confidential data securely and compliantly. * Proficiency in ...

Senior Clinical Data Manager

Somerset, NJ ยท On-site

$90K - $100K/yr

Position: Senior Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $90,000 to $100,000 About Pharmaron Pharmaron is a global CRO (Contract Research ...

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How much do associate clinical data manager jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for associate clinical data manager in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

What does an Associate Clinical Data Manager do?

An Associate Clinical Data Manager is responsible for collecting, cleaning, and managing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They work closely with clinical teams to design data collection tools, monitor data quality, and resolve discrepancies. Their work is crucial in supporting the analysis and reporting of clinical trial results, which can impact decisions about new medical treatments.

What are the key skills and qualifications needed to thrive as an Associate Clinical Data Manager, and why are they important?

To thrive as an Associate Clinical Data Manager, you need a solid background in life sciences or related fields, strong analytical abilities, and attention to detail, often supported by a relevant bachelor's degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools like Medidata Rave, and an understanding of regulatory guidelines such as ICH-GCP are typically required. Excellent organizational skills, effective communication, and problem-solving abilities help you excel in managing complex datasets and collaborating across teams. These skills ensure data integrity, regulatory compliance, and smooth conduct of clinical trials, which are critical to successful drug development.

What are some common challenges an Associate Clinical Data Manager might face when working on multi-site clinical trials?

Associate Clinical Data Managers often encounter challenges such as ensuring data consistency across different trial sites and managing discrepancies that arise from varying data entry practices. Coordinating with site staff, monitoring data quality, and adhering to strict timelines require strong communication and organizational skills. Additionally, adapting to evolving regulatory requirements and new data management technologies can be demanding, but these challenges also offer valuable learning opportunities for career growth.
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Clinical Data Manager

Clinical Data Manager

TScan Therapeutics

Waltham, MA โ€ข On-site

$130K - $150K/yr

Full-time

Re-posted 23 days ago


Job description

TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for looking for a Clinical Data Manager to support data management activities across our studies in solid tumors and hematological tumors. Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy fast-paced, collaborative, and vibrant culture. A team player with a sense of urgency will thrive in this role.
Responsibilities:
  • Lead all study specific data management activities with internal and external stakeholders.
  • Work with CROs in designing and updating CRFs, EDC systems and edit checks
  • Develop data management documents to support study execution (e.g. Data Management Plans, eCRF completion guidelines, Data Review Plans, etc)
  • Oversee internal and external database cleaning, query resolution and database lock activities
  • Support SAE reconciliation and medical coding activities
  • Develop data transfer agreements with third parties
  • Generate ad hoc data listings to support medical, clinical operations and translational research activities (e.g. listings to support Safety Review Meetings or Dose Escalation Meetings, consolidating translational data sets, etc

Requirements:
  • Bachelor's degree required
  • 5 -8 years of experience managing data management activities to support oncology clinical studies
  • Excellent communication skills and ability to work in a flexible, matrix environment
  • Experience managing external resources such as vendors and CROs
  • Advanced working knowledge of all relevant guidelines, including ICH, GCP, and other relevant FDA guidance's
  • Excellent oral and written business communication skills
  • Ability to drive a team-oriented environment, motivate and influence others, lead strategic discussions and interact with critical internal and external stakeholders

About TScan:
TScan Therapeutics is a fully integrated, next-generation TCR-T cell therapy company. Founded in 2018, TScan's platform was developed by Stephen Elledge, Ph.D., and Tomasz Kula, Ph.D., at Brigham and Women's Hospital and Harvard Medical School. TScan's transformative platform enables rapid discovery of TCRs and targets for engineered T cell therapy. This technology is extremely versatile and is applicable across multiple therapeutic areas beyond cancers, including autoimmune disorders and infectious diseases.
Do YOU have the anatomy of a TScanner?
Our talented, compassionate, and intelligent team is what makes TScan a Top Place to Work (as ranked by The Boston Globe). Our state-of-the-art offices with over 70,000 square feet of premium lab space, including an internal GMP manufacturing suite, are an environment that supports innovation, camaraderie, and professionalism. We are passionate, fun, flexible, and team oriented. Sound like you? Apply today.
EEO Statement
TScan is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, citizenship status, sexual orientation, gender identity or expression, or any other characteristic identified by federal, state, or local laws where we operate. TScan provides reasonable accommodations to qualified applicants and employees with disabilities. To begin an interactive dialogue with TScan regarding a reasonable accommodation in connection with the hiring process and/or to perform the responsibilities of the position for which the applicant has applied, please contact the recruiter.
Pay Range: $130,000-$150,000
Pay Transparency
TScan Therapeutics' pay ranges are established based on external market data from third-party compensation surveys and our internal benchmarking. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Individual compensation within this range is commensurate with a candidate's specific qualifications, including education, overall experience, relevant experience, and specific skills. We strive to ensure that compensation is competitive, equitable, and aligned with the value each TScanner brings to the role.
Recruitment & Staffing Agencies
TScan Therapeutics does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics' internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of TScan Therapeutics, and TScan Therapeutics will not owe any referral or other fees with respect thereto.