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Clinical Data Management Jobs in Reston, VA (NOW HIRING)

Emmes

Principal Clinical Data Manager

Rockville, MD · On-site

$150 - $200/hr

Overview Principal Clinical Data Manager Location: Remote About This Opportunity: This is an ... Data Management Handbook, Data Management Plan, Data Validation Plan, EDC System User's Guide, EDC ...

Peers and Partners

Clinical Data Manager

Bethesda, MD · On-site

CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...

Syneos Health, Inc.

Project Data Manager

Washington, DC · On-site

$100 - $125/hr

Clinical data management experience or an equivalent combination of education and experience. * Experience of Clinical Data Management practices and relational database management software systems.

CRi

Clinical Data & Applications Analyst II

Chantilly, VA · On-site

$65K - $70K/yr

Description Clinical Data & Applications Analyst - Onsite role based in Chantilly, VA Position Summary CRi is seeking a Clinical Data & Applications Analyst to support the management, optimization ...

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Clinical Data Management information

See Reston, VA salary details

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$60

$86

How much do clinical data management jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for clinical data management in Reston, VA is $60.42, according to ZipRecruiter salary data. Most workers in this role earn between $47.74 and $71.88 per hour, depending on experience, location, and employer.

What is clinical data management?

Clinical data management (CDM) is a critical process in clinical research that involves collecting, cleaning, and managing data generated during clinical trials. The goal is to ensure that the data is accurate, reliable, and compliant with regulatory standards. CDM professionals work closely with researchers, statisticians, and regulatory bodies to validate data and ensure its integrity throughout the study. This process helps in making informed decisions about the safety and efficacy of new drugs or treatments.

What are the key skills and qualifications needed to thrive in clinical data management?

To thrive in Clinical Data Management, you need a strong background in life sciences, attention to detail, and understanding of clinical trial processes, often supported by a relevant degree. Familiarity with industry-standard data management systems such as Medidata Rave or Oracle Clinical, as well as knowledge of CDISC standards and regulatory requirements, is essential. Excellent organizational skills, communication, and problem-solving abilities help ensure data integrity and effective cross-functional collaboration. These skills and qualities are crucial for ensuring high-quality, compliant data that supports clinical research and regulatory submissions.

What are some common challenges faced by professionals in clinical data management, and how can they be addressed?

One of the common challenges in Clinical Data Management is ensuring data accuracy and consistency across multiple sources and formats. This often involves resolving discrepancies and managing large volumes of data within tight timelines. Effective communication with clinical research associates, statisticians, and IT teams is crucial to address data queries promptly and maintain data integrity. Staying updated with regulatory requirements and leveraging advanced data management systems can also help mitigate these challenges and improve overall workflow efficiency.

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

AspectClinical Data ManagementClinical Data Coordinator
ResponsibilitiesDesigning data collection processes, database setup, data validation, and ensuring data quality for clinical trials.Collecting, reviewing, and entering clinical trial data, ensuring accuracy and completeness.
Required SkillsKnowledge of data management systems, clinical trial processes, and data validation techniques.Attention to detail, data entry skills, familiarity with clinical trial documentation.
Work EnvironmentTypically in clinical research organizations, pharmaceutical companies, or CROs.Often within clinical sites or research teams supporting data collection activities.

While both roles focus on clinical trial data, Clinical Data Management involves designing and overseeing data systems and ensuring data integrity, whereas Clinical Data Coordinators handle the day-to-day data collection and entry tasks. Both are essential for successful clinical research but differ in scope and responsibilities.

How do I become a clinical data management?

To become a clinical data manager, typically a bachelor's degree in life sciences, healthcare, or related fields is required. Gaining experience with clinical trial processes, data management tools like EDC systems, and obtaining certifications such as the Society for Clinical Data Management (SCDM) certification can enhance job prospects.

What are popular job titles related to Clinical Data Management jobs in Reston, VA?

For Clinical Data Management jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Clinical Data Management jobs in Reston, VA look for?

The top searched job categories for Clinical Data Management jobs in Reston, VA are:

What cities near Reston, VA are hiring for Clinical Data Management jobs?

Cities near Reston, VA with the most Clinical Data Management job openings:

Clinical Data Management jobs near you
Infographic showing various Clinical Data Management job openings in Reston, VA as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $123,707 per year, or $59.5 per hour.

Senior Manager, Clinical Data Management

Gaithersburg, MD

BioNTech SE
See more jobs at BioNTech SEexternal

$130K - $209K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 27 days ago

Key responsibilities

  • Serve as the primary point of contact for partners and sub-contractors on data management deliverables and activities

  • Supervise clinical data management tasks, negotiating timelines, processes, and addressing quality issues directly with CROs

  • Organize and oversee clinical data management activities aligned with BioNTech's strategy and standards

Job description

Cambridge, US; Gaithersburg, US; New Jersey, US   |   full time   |   Job ID: 11678 

About the role:

At BioNTech, we are more than a biotechnology company - we are a community of innovators dedicated to revolutionizing medicine. As a Senior Manager Clinical Data Management, you will play a pivotal role in ensuring the integrity and quality of clinical data that drives groundbreaking research and development. You will be at the forefront of managing data processes that contribute to advancing our diversified portfolio of product candidates. Join us in shaping the future of medicine within an environment that values collaboration, innovation, and diversity.

Your contribution:

  • Serve as the primary point of contact for partners and sub-contractors on data management deliverables and activities
  • Provide technical expertise while collaborating with CRO data managers for end-to-end clinical data management activities
  • Supervise clinical data management tasks, negotiating timelines, processes, and addressing quality issues directly with CROs
  • Organize and oversee clinical data management activities aligned with BioNTech's strategy and standards
  • Participate in protocol development, creating and validating essential documents such as CRFs and validation plans
  • Ensure compliance with Good Clinical Practices (GCPs) and regulatory guidelines while supporting medical review processes

A good match:

  • University degree in natural/life sciences or equivalent experience in Clinical Data Management within CRO/biotechnology/pharmaceutical settings with 7-10 years of experience in Clinical Data Management,
  • Profound knowledge of international guidelines (ICH-GCP) for clinical research projects
  • Experience with Clinical Database Systems like Medidata or OCRDC along with proficiency in MS Office tools (Word, Excel, PowerPoint)
  • Excellent organizational skills, attention to detail, and ability to work independently while being proactive
  • Strong communication skills paired with a team-oriented mindset

At BioNTech, your work has the potential to impact lives globally. Apply today to become part of our mission-driven team!

Your benefits and remuneration:

Expected Pay Range: $130,800/year to $209,400/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.

BioNTech US is committed to employee wellbeing and offers best-in-class benefits & HR programs to support an inclusive & diverse workforce. Salaried/Position-Targeted Hourly Employees working 30+ hours per week are eligible for our comprehensive benefits package. Benefits include but are not limited to:

  • Medical, Dental and Vision Insurance
  • Life, AD&D, Critical Illness Insurance
  • Pre-tax HSA & FSA, DCRA Spending Accounts
  • Employee Assistance & Concierge Program (EAP) available 24/7
  • Parental and Childbirth Leave & Family Planning Assistance
  • Sitterstream: Virtual Tutoring & Childcare Membership
  • Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.
  • 401(K) Plan with Company Match
  • Tuition Reimbursement & Student Loan Assistance Programs
  • Wellbeing Incentive Platforms & Incentives
  • Professional Development Programs
  • Commuting Allowance and subsidized parking
  • Discounted Home, Auto & Pet Insurance

...and more! More details to be shared.
 

Home to dozens of research institutions, biopharmaceutical companies, life science incubators, venture capital firms, and over 30 million square feet of laboratory space, Cambridge, Massachusetts has earned a reputation as the #1 life science cluster in the world. As part of the Greater Boston area, the city is often referred to as the "biotech supercluster" due to its high concentration of life sciences firms. This unique ecosystem is the result of a model partnership between academia and industry, fostering collaboration and innovation and driving the development of new therapies, medical devices, and diagnostics. As Cambridge's thriving life sciences industry continues to evolve, the city remains a beacon of knowledge, innovation, and collaboration, poised to shape the future of science and technology.

Apply now - We look forward to your application!

Apply for our Cambridge, US; Gaithersburg, US; New Jersey, US location and simply send us your documents using our online form.

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.

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