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Associate Clinical Data Manager Jobs in Colmar, PA

Position Summary The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data ...

Associate degree with a minimum of 3 years' experience working in clinical data programming, data engineering, or related data-management/clinical operations functions OR * Bachelor's Degree with a ...

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Associate Clinical Data Manager information

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

As of Aug 27, 2026, the average hourly pay for associate clinical data manager in Colmar, PA is $38.54, according to ZipRecruiter salary data. Most workers in this role earn between $29.04 and $38.51 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?

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.

What are popular job titles related to Associate Clinical Data Manager jobs in Colmar, PA?

For Associate Clinical Data Manager jobs in Colmar, PA, the most frequently searched job titles are:

What cities near Colmar, PA are hiring for Associate Clinical Data Manager jobs?

Cities near Colmar, PA with the most Associate Clinical Data Manager job openings:

Infographic showing various Associate Clinical Data Manager job openings in Colmar, PA as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $80,170 per year, or $38.5 per hour.

Clinical Data Manager

American College of Radiology

Philadelphia, PA • On-site

Full-time

Retirement, PTO

Posted 9 days ago


Job description

The American College of Radiology is a professional association serving over 40,000 members nationwide.  Consistent with the ACR’s mission to advance the practice of radiology and improve the health outcomes of the populations we serve, the ACR’s Center for Research and Innovation (CRI) has been a world leader in radiology clinical research for over 50 years.  Over this period, the CRI has conducted clinical research trials and other research projects that have transformed the practice of radiology, informed the development of clinical practice standards, led to new device approvals, and changed healthcare policy.

The CRI is the core radiology resource for NCI multicenter clinical trials involving diagnostic or therapeutic radiology.  And through active research committees in neuroradiology, cardiology, oncology, and pediatrics, the CRI has developed and delivered a diverse range of research studies in partnerships with academia and commercial sponsors.  Research studies range from prospective clinical trials to retrospective reader studies, novel imaging methods and imaging software, validation of biomarkers, radiomic feature analysis, and AI algorithm development and validation.

As a Clinical Data Manager, you will play a critical role in the design, implementation, and management of clinical trial databases and data collection systems. Working closely with investigators, project teams, and data programmers, you will help ensure the integrity, quality, and usability of study data from initiation through study completion.

As a member of the ACR team, you will:

  • Review study protocols and lead clinical data management activities during study startup.
  • Design data collection strategies aligned with protocol objectives and study endpoints.
  • Collaborate with investigators and research teams to develop metadata and data capture specifications.
  • Partner with Clinical Data Programming staff to configure and validate electronic data capture (EDC) systems.
  • Develop edit checks, web logic, and validation specifications to promote data quality and consistency.
  • Create study calendars and data collection schedules.
  • Conduct Operational Qualification (OQ) and Performance Qualification (PQ) testing of databases and study systems.
  • Develop case report form (CRF) completion guidelines and user documentation.
  • Produce standard, study-specific, and ad hoc reports to support study oversight and decision-making.
  • Define and document database modifications required to support protocol amendments and study changes.
  • Perform quality control reviews to ensure data accuracy, completeness, and regulatory compliance.
  • Serve as a trusted resource for site research staff, providing guidance on protocol requirements and data collection procedures.

Qualified candidates will possess the following:

  • 3+ years of related experience preferred.
  • Professional nursing degree/other healthcare certification/bachelor’s degree preferred.
  • Experience in a multi-modality clinical trials group or research team a plus.
  • Knowledge of CDASH/CDISC Standards a plus.
  • Experience with electronic data capture (EDC) platforms required.
  • Certified Medidata Rave® Study Builder a plus.
  • Strong attention to detail and commitment to data quality and process excellence required.
  • Excellent organizational, communication, and collaboration skills required.
  • Ability to manage multiple priorities in a fast-paced, team-oriented environment required.

If you would like to put your experience to great use in a professional team-oriented environment, please apply online. To learn more about ACR’s rewarding employee experience, culture, and benefits, visit: https://www.acr.org/About-ACR/Work-With-Us

ACR is committed to a total rewards compensation philosophy that includes base salary in addition to our full suite of comprehensive benefits.  ACR’s goal is to pay competitively and equitably.  It is typical for individuals to be hired in the entry to middle of the range for their role, and compensation decisions depend on each case’s circumstances.  A reasonable estimate of the annual compensation range for this position is 73-80k.  

ACR offers a rewarding employee experience: innovative culture, professional growth potential, competitive compensation, and an exceptional benefits package, including a defined contribution pension plan, 403(b); generous paid time off package; insurance plans with the leading providers; flexible spending; tuition reimbursement; training opportunities; and wellness reimbursement.