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Associate Clinical Data Manager Jobs (NOW HIRING)

Pharmaron

Senior Clinical Data Manager

Somerset, NJ

$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 ...

Iterative Health

Clinical Data Manager

Cambridge, MA

$97K - $120K/yr

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

Pharmaron

Senior Clinical Data Manager

Somerset, NJ · 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 ...

Cooper Companies

Lead Clinical Data Manager

San Ramon, CA · Hybrid

$164K - $219K/yr

Leads all aspects of clinical data management activities from study initiation through database lock and study closeout. Develops, optimizes and controls data management system, including external ...

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

As of Jun 20, 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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Associate Clinical Data Manager jobs near you
Senior Clinical Data Manager

Senior Clinical Data Manager

Pharmaron

Somerset, NJ

$90K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 23 days ago

Job description

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 Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit www.pharmaron.com.

We are seeking an experienced Senior Clinical Data Manager to lead and oversee data management activities across clinical trials while ensuring the integrity, accuracy, and reliability of clinical data. This role is responsible for managing all phases of clinical data management, including study start-up, CRF design, database set-up, edit check specifications, vendor oversight, data cleaning, and database lock activities, while maintaining compliance with GCP, CDISC standards, regulatory requirements, and company SOPs.

The ideal candidate will serve as Lead Data Manager for assigned studies, coordinating resources, managing timelines and deliverables, collaborating with internal teams, sponsors, and vendors, and supporting audits and inspections. The Senior Clinical Data Manager will also contribute to process improvements, mentor team members, and provide risk management guidance to ensure high-quality project execution aligned with client expectations.

Responsibilities:

  • Ensure the integrity, reliability, and accuracy of clinical trial data.
  • Maintain clinical data quality and consistency in line with regulatory requirements, SOPs, processes, and data standards.
  • Verify external data conforms to data transfer specifications.
  • Ensure all data management activities comply with GCP, regulatory requirements, and Pharmaron Clinical/Sponsor SOPs.
  • Apply CDISC or applicable standards to data/database programming throughout the trial.
  • Adhere to Pharmaron Clinical policies and procedures.
  • Act as Lead Data Manager for clinical trials: arrange resources, assess workload, define study scope, and create timelines.
  • Oversee all data management tasks for assigned trials; monitor deliverables to meet timelines and quality standards.
  • Participate in internal/external meetings, audits, and regulatory inspections.
  • Communicate effectively with internal teams, vendors, and clients; provide risk management assessments.
  • Mentor and train team members; perform data management tasks as needed.
  • Lead project teams to deliver services aligned with client needs and contractual obligations.
  • Develop and improve clinical data management SOPs and processes; recommend improvements to senior management.

What We're Looking For:

  • Bachelor's Degree with at least 4 years' experience within a data management role, understanding of processes including study management, vendor management, CRF design, database set-up, edit check specification, DMPs, and data cleaning activities up to and including database lock.
  • Demonstrated knowledge of the functions and activities of clinical trials.
  • Demonstrated knowledge of GCP and other regulatory requirements for clinical trials.
  • CRO experience strongly preferred.

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:

  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

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