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Remote Clinical Trials Data Analyst Jobs in Virginia

Booz Allen Hamilton, Inc.

Data Analyst

Arlington, VA · On-site +1

Remote Work: Hybrid Job Number: R0247289 Location: Arlington,VA,US Share job via: Share Data Analyst The Opportunity: As data analyst, you love diving into data and turning it into meaningful ...

Booz Allen Hamilton, Inc.

Data Analyst

Arlington, VA · On-site +1

$62K - $141K/yr

Remote Work: No Job Number: R0247514 Location: Arlington,VA,US Share job via: Share Data Analyst The Opportunity: As data analyst, you love diving into data and turning it into meaningful insights.

IQVIA

Senior Data Team Lead (Remote)

Richmond, VA · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

Redhorse Corporation

Data Analyst

Arlington, VA · On-site +1

Data Analyst About the Organization Now is a great time to join Redhorse Corporation. Our mission ... for remote work to be determined by the program manager and customer. Essential Functions:

IQVIA

Senior Data Team Lead (Remote)

Virginia Beach, VA · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

IQVIA

Senior Data Team Lead (Remote)

Norfolk, VA · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

Ansible Government Solutions

Senior Data Analyst

Arlington, VA · On-site +1

$98K - $124K/yr

Overview The Senior Data Analyst supports the Veterans Health Administration Specialty Care Program ... The work is fast-paced and highly collaborative, requiring strong clinical informatics expertise ...

TSTC

Junior Data Analyst

Arlington, VA · On-site +1

$50K - $75K/yr

TSTC is seeking a full-time Junior Data Analyst to provide research services for one of TSTC ... Flexible Work Options - Remote work allowed, flexible schedules, and telework opportunities ...

TSTC

Junior Data Analyst

Arlington, VA · On-site +1

$50K - $75K/yr

TSTC is seeking a full-time Junior Data Analyst to provide research services for one of TSTC ... Flexible Work Options - Remote work allowed, flexible schedules, and telework opportunities ...

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All JobsClinical Trials Data Analyst JobsRemote Clinical Trials Data Analyst JobsRemote Clinical Trials Data Analyst Jobs in Virginia

Remote Clinical Trials Data Analyst information

What is the difference between Remote Clinical Trials Data Analyst vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trials Data AnalystRemote Clinical Research Coordinator
Primary RoleAnalyzes clinical trial data, manages databases, generates reportsCoordinates trial activities, manages site operations, ensures protocol compliance
Required SkillsData analysis, statistical software, attention to detailCommunication, organization, regulatory knowledge
Work EnvironmentRemote, primarily computer-basedRemote or onsite, site management
Common CertificationsCertified Clinical Data Manager (CCDM), related data certificationsCertified Clinical Research Professional (CCRP), site management certifications

The Remote Clinical Trials Data Analyst focuses on analyzing and managing clinical data remotely, while the Remote Clinical Research Coordinator handles trial coordination and site management. Both roles require understanding of clinical research but differ in daily tasks and skill sets.

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Remote Clinical Trials Data Analyst jobs near you
Infographic showing various Remote Clinical Trials Data Analyst job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 19% Part Time, and 2% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution.

Principal Biostatistician

Worldwide Clinical Trials

Triangle, VA • On-site, Remote

Full-time

Posted 6 days ago

Job description

Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What The Principal Scientist, Biostatistician does at Worldwide
Use independent judgment and technical expertise to assist in designing studies; preparing statistical analysis plans; analyzing data from pharmacokinetic, clinical, and pre-clinical studies; interpreting statistical results from pharmacokinetic, clinical, and related analyses; and generating randomization schedules for clinical studies.
Principal Scientists are recognized as scientific leaders in the company. They regularly contribute to literature and to building Worldwide Clinical Trials' intellectual property and are capable of leading interdisciplinary project teams.
What you will do
  • Accurately and efficiently perform tasks that are broad in scope

  • Use knowledge and judgment to reach well-defined goals in project management

  • Work independently and collaboratively to solve technical problems by implementing contemporary methods

  • Assist the clinic, method development, and marketing/business development by applying knowledge, conducting literature reviews, providing information, and offering related support

  • Train and guide less experienced personnel in techniques required for work assignments

  • Supervise personnel involved in statistical and pharmacokinetic-related work

  • Assist with the design of clinical studies and construct data analysis plans to meet study protocol requirements and maximize information from available data

  • Perform statistical analyses on clinical and pharmacokinetic data using appropriate methods and software programs

  • Prepare documentation for final reports, including text, tables, graphs, and analysis outputs

  • Interact with clients, bioanalytical personnel, and clinical personnel regarding study design, statistical analyses, pharmacokinetic data analyses, and data interpretation

  • Identify problems or potential problems in generating quality statistical and pharmacokinetic documents, report concerns to their supervisor, and propose possible solutions
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

What your bring to the role
  • Familiarity with corporate policies, goals, and objectives, normally acquired after three months of exposure to Worldwide Clinical Trials' operations

  • Understands and applies Good Laboratory Practice (GLP) guidelines and U.S. Food and Drug Administration (FDA) guidance documents pertinent to statistical analysis, pharmacokinetic studies, pharmacokinetic analyses, and reports

  • Excellent SAS programming skills

  • Proficient in the use of WinNonlin, nQuery, Microsoft Word, and Microsoft Excel

  • Ability to read, write, and understand complex literature

  • Ability to write concise, understandable study reports and communicate clearly with clients and Worldwide Clinical Trials personnel

  • Ability to create, understand, and interpret graphs, tables, and charts

  • Strong organizational and problem-solving skills and ability to set priorities

  • Ability to interact effectively with superiors, peers, and others and communicate ideas clearly

  • Ability to follow and implement Worldwide Clinical Trials' policies and Standard Operating Procedures, normally associated with three months of experience at Worldwide Clinical Trials

Your experience
  • PhD or postgraduate degree with a scientific focus preferred

  • Bachelor's degree with a scientific focus and 12 or more years of relevant work experience required

Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $96,500.00 - $191,500.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

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