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Senior Clinical Data Associate Jobs (NOW HIRING)

Unlearn

Senior Clinical Data Scientist

San Francisco, CA · On-site

$160K - $180K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Senior Clinical Data Scientists at Unlearn build world-class data products that underpin advances in machine learning for clinical research. Working in close collaboration with machine learning ...

Fortrea

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and training to DM to ensure best working practices are maintained. Summary of Responsibilities:

Fortrea

Sr. Clinical Data Manager

Durham, CA · On-site

$120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and training to DM to ensure best working practices are maintained. Summary of Responsibilities:

Fortrea

Sr. Clinical Data Manager

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and training to DM to ensure best working practices are maintained. Summary of Responsibilities:

Fortrea

Senior Clinical Data Manager

Durham, NC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and training to DM to ensure best working practices are maintained. Summary of Responsibilities:

Karius

Senior Clinical Data Scientist

Redwood City, CA · On-site +1

$200K/yr

Position Summary The Sr. Clinical Data Scientist will serve as the primary data architect for Karius's large-scale commercial real-world evidence registry. This role sits at the intersection of ...

Fortrea

Senior Clinical Data Manager

Durham, CA · On-site

$120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and training to DM to ensure best working practices are maintained. Summary of Responsibilities:

Karius

Senior Clinical Data Scientist

Redwood City, CA · On-site +1

Position Summary The Sr. Clinical Data Scientist will serve as the primary data architect for Karius's large-scale commercial real-world evidence registry. This role sits at the intersection of ...

Karius

Senior Clinical Data Scientist

Redwood City, CA · On-site

$133.82 - $200.74/hr

Position Summary The Sr. Clinical Data Scientist will serve as the primary data architect for Karius's large‑scale commercial real‑world evidence registry. This role sits at the intersection of ...

Icon plc

Senior Clinical Research Associate

Blue Bell, PA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Performing data review and resolution of queries to maintain high-quality clinical data ... for a Senior Clinical Research Associate. * In-depth knowledge of clinical trial processes ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Performing data review and resolution of queries to maintain high-quality clinical data ... for a Senior Clinical Research Associate. * In-depth knowledge of clinical trial processes ...

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How much do senior clinical data associate jobs pay per year?

As of Aug 15, 2026, the average yearly pay for senior clinical data associate in the United States is $58,937.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,000.00 and $67,500.00 per year, depending on experience, location, and employer.

What are some common challenges senior clinical data associates face when managing large clinical trial datasets?

Senior Clinical Data Associates often manage complex datasets from multiple sites, which can lead to challenges such as ensuring data consistency across sources, resolving discrepancies, and maintaining data integrity under tight timelines. Additionally, they must stay up-to-date with evolving regulatory requirements and work closely with cross-functional teams, including biostatisticians, clinical operations, and data managers, to ensure accurate and timely data delivery. Effective communication, attention to detail, and adaptability are essential to overcome these challenges and ensure successful trial outcomes.

What are the key skills and qualifications needed to thrive as a senior clinical data associate?

To thrive as a Senior Clinical Data Associate, you need expertise in clinical data management, data cleaning, and knowledge of clinical trial processes, supported by a degree in life sciences or a related field. Familiarity with data management systems like Medidata Rave, EDC platforms, and certifications such as CCDM are commonly required. Attention to detail, strong analytical thinking, and effective communication skills help you excel in ensuring data accuracy and collaborating with cross-functional teams. These capabilities are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical research studies.

What does a senior clinical data associate do?

A Senior Clinical Data Associate is responsible for managing and ensuring the accuracy, integrity, and quality of data collected during clinical trials. They oversee data collection processes, review case report forms, resolve data discrepancies, and ensure compliance with regulatory standards. In addition to performing data management tasks, Senior Clinical Data Associates often mentor junior staff, contribute to developing data management plans, and collaborate with clinical research teams to ensure successful trial outcomes.

What cities are hiring for Senior Clinical Data Associate jobs?

Cities with the most Senior Clinical Data Associate job openings:

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Senior Clinical Data Associate jobs near you

Sr. Manager, Clinical Data Management

Moderna, Inc.

Cambridge, MA • On-site

$130K - $209K/yr

Full-time

Medical, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Moderna rating

9.2

Company rating: 9.2 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

5th of 86 rated pharmaceutical

Job description

The Role:
Moderna Services, Inc. seeks a Sr. Manager, Clinical Data Management for its Cambridge, Massachusetts location.
Here's What You'll Do:
  • Lead data management activities for in-house and outsourced studies.
  • Responsible for vendor oversight activities across global development programs.
  • Represent data management function in clinical cross-functional meetings, ensuring aligned expectations between the Contract Research Organization (CRO) and Moderna for all data related deliverables, especially in support of key decision points and regulatory submissions.
  • Ensure established milestones and deliverables are met with the highest degree of quality.
  • Partner with appropriate stakeholders and CRO partners to mitigate and resolve risks.
  • Provide input to functional governance with Moderna strategic suppliers.
  • Partner with appropriate stakeholders to resolve issues escalated from the vendor and/or cross-functional teams.
  • Lead and manage clinical trial data collection set-up, data review, and database lock for studies where data management activities are conducted within Moderna.
  • Work with other functions to complete set up of Electronic Data Capture (EDC) and study data collection tools such as Inter-response time (IRT), ePRO and eCOA.
  • Lead the creation and maintenance of study cross functional data review plan components, including edit checks (data validation plan), listing review checks, data integration specifications, data transfer specifications, external data reconciliation plans, coding guidelines, Serious Adverse Events (SAE) reconciliation guidelines, and database lock plans.
  • Lead data review, including query management, and activities required for interim and final database locks.
  • Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents.
  • Ensure achievement of major data management deliverables and milestones in coordination with the Clinical Operations Clinical Development, Biostatistics & Programming, Biomarker Operations & Sample Management and Pharmacovigilance.
  • Plan and manage external Data Management budgets and timelines to ensure accuracy, understand trends in variances and support continuous improvement in forecasting.
  • Act as a process expert for operational and oversight models.
  • Maintain Standard Operating Procedures (SOPs), process maps and templates and timelines to support functions operational and oversight models.
  • May prepare metrics to support the function Key Performance Indicators (KPIs).
  • Represent function in external professional initiatives and organizations such as SCDM, CDISC, and DIA to identify industry best practice and increase the visibility of Moderna.
  • Lead functional Continuous Improvement initiatives, providing strategic direction and identifying key deliverables that meet timelines, budget, and are in alignment with requirements.
  • Work cross-functionally to ensure the quality of the data in each database and on time delivery, as well as quality of other data management deliverables.
  • Champion and adopt technology improvements and tools for use in clinical data management processes.
  • Ensure compliance with own Learning Curricula, corporate and GXP requirements.

Here's What You'll Bring to the Table:
Minimum requirements:
  • Requires a Bachelor's degree, or foreign equivalent, in Biotechnology, Biology, Biological Sciences, or related field and 8 years of progressive, post-baccalaureate experience as a Sr. Manager, Assistant Clinical Data Manager, Clinical Data Associate or related position supporting clinical data management for the pharmaceutical industry.
  • 7 years of experience must include:
    • Vendor Management;
    • Medidata RAVE, InForm, and Oracle Clinical EDC tools;
    • Clinical Data Management using Biomarker and External data;
    • Utilizing eTMF tools;
    • Study Database Lock processes including Final, Interim, Snapshots, DSUR submission, and Staggered Lock;
    • Study Initiation, CSR Review, and SAE Reporting;
    • J-Review, I-Review, and Clinbrowser; and
    • SDTM and CDISC datasets, Clinical Data Studio, SQL & SAS.
  • 100% telecommuting permitted from anywhere within the US.

The salary range for this role is $130,800 to $209,400. This range reflects the lowest to highest salary we, in good faith, believe we would pay for this role at the time of this posting. The minimum target pay for this particular position, based on its primary location, is $196,400 to $209,400. An individual's placement within the range will depend on several factors, including but not limited to specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.
Apply at https://modernatx.wd1.myworkdayjobs.com/en-US/M_tx (Job ID: R19409) or email resume and cover letter to careers@modernatx.com with subject line: R19409.
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That's why our US benefits and global well-being resources are designed to support you-at work, at home, and everywhere in between.
  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities to help you plan for the future
  • Location-specific perks and extras

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.
#dni
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That's why our benefits and well-being resources are designed to support you-at work, at home, and everywhere in between.
  • Competitive healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

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About Moderna

Sourced by ZipRecruiter

In just over a decade, Moderna has evolved from a research-focused company in the messenger RNA (mRNA) field to a leading enterprise with a diverse clinical portfolio of vaccines and therapeutics. With a strong intellectual property portfolio and state-of-the-art manufacturing capabilities, Moderna collaborates with global partners to advance groundbreaking science and achieve rapid scaling of production. Notably, Moderna's mRNA platform has enabled the development of therapies for various diseases, including infectious diseases, immuno-oncology, and cardiovascular conditions. Recognized as a top biopharmaceutical employer, Moderna fosters an inclusive and smoke-free work environment. The company is dedicated to equal employment opportunities and non-discrimination, ensuring that all employees and applicants are treated with respect and without bias based on factors like race, gender, religion, disability, or sexual orientation. Moderna is also committed to providing reasonable accommodations for individuals with disabilities, in accordance with applicable laws. To know more, visit www.modernatx.com.

Industry

Manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

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