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Clinical Data Management Associate Jobs in Reading, MA

Manager, Clinical Data Management

Boston, MA ยท On-site

$99K - $166K/yr

Partner with internal and external stakeholders to optimize Data Management technology, processes ... programming to ensure clinical databases are designed in a standard, accurate, complete, and ...

Manager, Clinical Data Management

Boston, MA ยท Remote

CA$99K - CA$166K/yr

Partner with internal and external stakeholders to optimize Data Management technology, processes ... programming to ensure clinical databases are designed in a standard, accurate, complete, and ...

Clinical Data Manager

Burlington, MA ยท On-site

$145K - $160K/yr

... Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role in ensuring the integrity, accuracy, and completeness of clinical trial data ...

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Showing results 1-20

Clinical Data Management Associate information

See Reading, MA salary details

$14

$41

$91

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

As of Jul 30, 2026, the average hourly pay for clinical data management associate in Reading, MA is $41.10, according to ZipRecruiter salary data. Most workers in this role earn between $30.96 and $41.11 per hour, depending on experience, location, and employer.

Which is better, CDM or SAS?

For a Clinical Data Management Associate, SAS is a widely used statistical software for data analysis and reporting, while CDM refers to the role of managing clinical data, often involving tools like electronic data capture systems. Both are important in clinical trials, but SAS skills are highly valued for data analysis tasks, whereas CDM focuses on data collection, validation, and database management.

Is clinical data management a good career?

Clinical Data Management Associate roles involve collecting, cleaning, and maintaining clinical trial data, requiring knowledge of databases and regulatory standards. It offers opportunities for growth in the pharmaceutical and healthcare industries, with a demand for strong analytical and technical skills. The field provides a stable career path with potential for advancement and specialization.

What does a clinical data associate do?

A Clinical Data Management Associate is responsible for collecting, cleaning, and maintaining clinical trial data to ensure accuracy and compliance. They use data management tools and work closely with research teams to support the integrity of trial results and may require knowledge of regulatory standards like GCP and data validation techniques.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically an entry-level to mid-level position in clinical trials, often requiring a bachelor's degree in a related field and some experience in clinical research or monitoring. Entry-level CRAs usually undergo training and may need certifications such as SOCRA or ACRP to advance in the role.

What is the difference between Clinical Data Management Associate vs Clinical Data Coordinator?

AspectClinical Data Management AssociateClinical Data Coordinator
ResponsibilitiesData entry, validation, database management, ensuring data qualityOversees data collection, manages databases, coordinates data flow between teams
Required SkillsAttention to detail, knowledge of clinical data systems, basic understanding of regulationsStrong organizational skills, data management experience, communication skills
Work EnvironmentClinical research labs, CROs, pharmaceutical companiesClinical trial sites, research organizations, CROs
Common UsageEntry to mid-level data roles in clinical trialsData oversight and coordination roles in clinical studies

The Clinical Data Management Associate focuses on data entry, validation, and database management, ensuring data accuracy. The Clinical Data Coordinator oversees data collection and flow, coordinating between teams. Both roles require similar skills and work environments but differ in scope and responsibilities.

What cities near Reading, MA are hiring for Clinical Data Management Associate jobs? Cities near Reading, MA with the most Clinical Data Management Associate job openings:

Director, Clinical Data Management

Alnylam Pharmaceuticals

Cambridge, MA โ€ข On-site

$197K - $266K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago


Job description

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Summary

The Director, Clinical Data Management is responsible for the oversight of data management activities in support of Alnylam studies across all stages of clinical drug development. This position reports to the head of the Clinical Data & Insights group.

Responsibilities:

  • Direct and grow internal data management expertise area, including management of direct reports;
  • Direct and establish standards for data management CRO outsourcing strategy and deliverables, including the CRO selection process and the governance of CRO performance;
  • Oversee the successful execution of all data management activities in support of Alnylam clinical studies in partnership with CROs, including eCRF development, database build, data collection, data coding, cleaning, database lock and archiving;
  • Supervise the execution of cross-functional, internal data review plans by direct reports across all Alnylam clinical studies;
  • Partner with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Clinical Pharmacology and Pharmacometrics, Bioanalytical, Safety & Risk Management (SRM) and Regulatory Affairs; CROs, central and local laboratories, and other vendors;
  • Lead development and implementation of data collection standards, consistent with industry best practice;
  • Lead data management contributions to the development of clinical protocols, clinical study reports and other regulatory documents, e.g. DSURs, Briefing Documents, etc.
  • Oversee development of department workflows, and infrastructure strategy and implementation, such as preferred provider initiatives, SOPs, and templates;
  • Collaborate with Statistical Programming and external vendors to ensure compliance of SDTM clinical datasets, consistent with CDISC standards;
  • Collaborate with Clinical Operations and Quality Assurance to certify the integrity and traceability of all clinical data sources, compliant with 21 CFR Part 11 standards;
  • Direct Data Management GCP inspection readiness efforts; function as a leader for Data Management in GCP inspections;
  • Represent Data Management at internal cross-functional meetings and external vendor leadership meetings;
  • Demonstrate clear alignment withAlnylam Core Valuesincluding, Commitment to People, Fiercely Innovative, Purposeful Urgency, Open Culture and Passion for Excellence.

Requirements

  • BS/BA in scientific discipline, MS or equivalent preferred, with at least 15 years of clinical data management experience in a pharmaceutical/biologics/biotechnology company, with at least 5 years in a leadership capacity;
  • Extensive experience managing global studies utilizing an outsourced CDM model from start-up through close-out;
  • Extensive experience managing direct reports and providing performance reviews and career development guidance;
  • Understanding ofICH GCP as well as general knowledge of industry practices and standards;
  • Knowledge and understanding of regulatory requirements and expectations for clinical data systems including 21 CFR Part 11;
  • Expert knowledge of eClinical processes, efficient design/build of an EDC data management system and other Clinical Trial data/Data Management Systems;
  • Expert knowledge and understanding of regulations and industry-adopted data standards, such as CDISC-SDTM and CDASH;
  • Experience using standardized medical terminology, including MedDRA and WHODrug;
  • Experience working with Medidata Rave EDC systems;
  • Experience working with elluminate or other data visualization systems a plus
  • Experience working with MS Office Suite (Excel, Word and PowerPoint) familiar with MS Project;
  • Excellent written and oral communication skills;
  • Highly motivated and flexible, with excellent organizational skills;
  • Ability to work independently and as part of a multi-disciplinary team.

#LI-AB1 #LI-Virtual

U.S. Pay Range

$197,200.00 - $266,800.00

The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).

Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.

Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers

AboutAlnylam

We are the leader in RNAi therapeutics- a revolutionaryapproach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possibleand are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, wherean authentic, inclusive culture and breakthrough thinkingfuel one another.

At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.

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