ZipRecruiter

Log In

1

Senior Clinical Data Standards Jobs in Reston, VA

Peers and Partners

Clinical Data Manager

Bethesda, MD · On-site

Review, organize, maintain, and manage clinical research data in accordance with established protocols, standard operating procedures (SOPs), and applicable Federal requirements. * Support data ...

Peers and Partners

Clinical Data Manager

Bethesda, MD · On-site

Review, organize, maintain, and manage clinical research data in accordance with established protocols, standard operating procedures (SOPs), and applicable Federal requirements. * Support data ...

ICON

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity ... Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs ...

Icon plc

Senior Clinical Research Associate

Washington, DC · Hybrid

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity ... Deliver training to ensure sitescomply withthe protocol, Standard Operating Procedures (SOPs), Good ...

REGENXBIO

Sr Clinical Project Manager

Rockville, MD · On-site

  • Retirement

Responsible for management of data management and clinical operations teams in review of clinical ... Maintains completion of required corporate training on standards, policies, work instructions by ...

REGENXBIO

Sr Clinical Project Manager

Rockville, MD · On-site

  • Retirement

Responsible for management of data management and clinical operations teams in review of clinical ... Maintains completion of required corporate training on standards, policies, work instructions by ...

next page

Showing results 1-20

All JobsClinical Data Standards JobsSenior Clinical Data Standards JobsSenior Clinical Data Standards Jobs in Reston, VA

Senior Clinical Data Standards information

See Reston, VA salary details

$41.1K

$61.3K

$76.5K

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

As of Aug 17, 2026, the average yearly pay for senior clinical data standards in Reston, VA is $61,315.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,900.00 and $70,200.00 per year, depending on experience, location, and employer.

What is the difference between Senior Clinical Data Standards vs Clinical Data Coordinator?

AspectSenior Clinical Data StandardsClinical Data Coordinator
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and experience in data standardsUsually requires a bachelor's degree in life sciences or related field
Work EnvironmentFocuses on developing, implementing, and maintaining data standards across clinical trialsManages data entry, validation, and coordination of clinical trial data collection
Employer & Industry UsageUsed in pharmaceutical, biotech, and CROs for data consistency and complianceCommonly employed in clinical research sites and sponsor companies for data management

While both roles are involved in clinical data, Senior Clinical Data Standards primarily develops and oversees data standards, whereas Clinical Data Coordinators focus on data collection and entry. Understanding these differences helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Data Standards jobs in Reston, VA?

The most popular types of Clinical Data Standards jobs in Reston, VA are:

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

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

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

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

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

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

Senior Clinical Data Standards jobs near you

Senior Clinical Data Manager

Supernus Pharmaceuticals, Inc.

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 18 days ago

Job description

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes.
Job Summary:
To provide leadership, strategic direction, and oversight for end-to-end clinical data management activities throughout the lifecycle of clinical trials - from study start-up through trial execution and study closeout - ensuring quality, compliant, and timely clinical data delivery.
Essential Duties & Responsibilities:
  • Lead all data management (DM) activities for one or more clinical trials.
  • Contribute to developing study protocols, statistical analysis plans, and clinical study reports.
  • Collaborate with Database Development on study database, eCRF, and edit checks design.
  • Manage user acceptance testing (UAT) of study database with cross-functional team members (including Clinical Operations, Clinical Development, Drug Safety, and Biostatistics).
  • Manage cross-functional collaboration with internal team members (from Clinical Operations, Clinical Development, Drug Safety, and Biostatistics) and external vendors (for trial conduct).
  • Develop and enforce study timeline for all DM and/or DM-related milestones.
  • Develop and enforce all DM-related plans, agreements, and guidelines (e.g., data management plan [DMP], data quality plan [DQC], data transfer agreement [DTA], and electronic CRF completion guidelines [eCCG]).
  • Collaborate with Document Management team to archive DM-related documents in Trial Master File (TMF).
  • Write DM-related SOPs and/or Job aids and contribute to improving DM processes.

Non-Essential Duties & Responsibilities:
  • Attends and participates in internal and external training sessions.

Supervisory Responsibilities:
  • May supervise Clinical Data Associates as needed.
  • Provides leadership or management in an effective manner consistent with Company Values towards defined Corporate Objectives.
  • Understands Company Policy and procedure to be able to guide direct reports appropriately, if applicable.

Knowledge & Other Qualifications:
  • Master's degree with at least 6 years or Bachelor's degree with at least 8 years of in pharmaceutical, CRO, Biotech, or health related field or industry.
  • Strong experience in data captures systems and clinical data review.
  • Strong knowledge of industry standards such as GCP, GCDMP, and CDISC (CDASH and SDTM).
  • Working knowledge of medical terminology and coding (MedDRA/WHO-Drug).
  • Working knowledge of data privacy rules in relation to clinical data management.
  • Nursing/medical/biology background is a plus.
  • Strong project and risk management skills with great attention to detail.
  • Excellent interpersonal and communication skills in English language (writing, speaking, and comprehending).
  • Computer literate with proficiency of Microsoft Office package including Word, Outlook, and Excel.

Other Characteristics:
  • Ability to work independently and as part of a team.
  • Ability to maintain high ethical standards of integrity and quality.
  • Capable of performing other duties as assigned by management.
  • Capable of being innovative and dynamic in approach to work.
  • Authorized to legally work in the United States without visa sponsorship.

Physical Requirements / Work Environment:
  • Sedentary work. Exerting up to 10 pounds of force occasionally and/or carrying objects. Sedentary work involves sitting most of the time.
  • The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer screen, iPad, or other electronic device; and extensive reading.
  • The worker is not substantially exposed to adverse environmental conditions.

Compensation:
At Supernus, we offer a competitive compensation package that reflects your experiences and contributions. The expected salary range for fully qualified candidates applying for this role is $145,000 to $160,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range may be modified in the future. An individual's salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.
You also will be able to participate in a competitive benefits package, including but not limited to: health, dental, vision, paid time off, 401k company match, company paid life insurance and health and wellness benefits. The total compensation package for this position also includes other compensation elements such as stock equity awards, employee stock purchase programs and participation in our Company's discretionary annual bonus program.
Supernus Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Apply