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Clinical Data Associate Jobs in Washington (NOW HIRING)

We sit at the intersection of clinical cardiology, hardware, software, and data, building products ... About the Role This role requires a detail-oriented and proactive Medical Billing Associate to ...

Research Nurse

Rockville, MD ยท On-site

$98 - $163/hr

Registered Nurse from an accredited associate's or bachelor's nursing program.* At least FOUR (4) years of experience.* Experience in clinical data management.* Familiarity with IRB and clinical ...

New

Research Nurse

Rockville, MD ยท On-site

$98K - $163K/yr

Registered Nurse from an accredited associate's or bachelor's nursing program. * At least FOUR (4) years of experience. * Experience in clinical data management. * Familiarity with IRB and clinical ...

Registered Nurse from an accredited associate's or bachelor's nursing program. * At least FOUR (4) years of experience. * Experience in clinical data management. * Familiarity with IRB and clinical ...

Senior Clinical Research Associate

Washington, DC ยท On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare ... This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity ...

As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and values ... Clinical Management, Regulatory Affairs, Data Management, and Statistical Programming. * Drive ...

Through our two business units-- Emmes, a full-service CRO , and Veridix AI, our technology, data ... The Senior Clinical Research Associate (CRA) is responsible for monitoring clinical study sites ...

Showing results 21-40

Clinical Data Associate information

See Washington salary details

$15

$44

$98

How much do clinical data associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical data associate in Washington is $44.12, according to ZipRecruiter salary data. Most workers in this role earn between $33.22 and $44.09 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Washington?

The most popular types of Clinical Data jobs in Washington are:

What are popular job titles related to Clinical Data Associate jobs in Washington?

For Clinical Data Associate jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Clinical Data Associate jobs in Washington look for?

The top searched job categories for Clinical Data Associate jobs in Washington are:

What cities in Washington are hiring for Clinical Data Associate jobs?

Cities in Washington with the most Clinical Data Associate job openings:

Infographic showing various Clinical Data Associate job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $91,763 per year, or $44.1 per hour.

Associate Project Leader - Vaccines & Infectious Diseases

The Emmes Company, LLC

Rockville, MD โ€ข On-site

Other

Medical, Retirement

Re-posted just now


Job description

Overview

Associate Project Leader

US Remote

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We're looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Asscoiate Project Leader (APL) is critical to the successful conduct of government-sponsored clinical research projects, serving as the matrix leader of the core project team. The APL is accountable for successful delivery of clients' statement of work activities within timeline and budget.


The APL develops and maintains a positive relationship with clients and other external stakeholders, oversees deliverable quality, and works collaboratively across departments to accomplish project goals. The APL is typically part of a large coorindating center team overseeing several protocols or activities in the larger coordinating center projeect.

The APL typically works under the direction of a more senior Leader, however the APL is responsible for the continuous monitoring, identification, escalation and mitigation of project risk for their assigned protocols/activities.


Responsibilities
  • Accountable for day-to-day execution of government research projects through collaboration with assigned projects' Emmes' project PI/Coordinating Center leader(s) and staff from other departments, including but not limited to Clinical Operations, Biostatistics, Clinical Data Management, Clinical Data Systems, Program Management, IT, Web Development, Finance, Contracts, Regulatory and Pharmacovigilance.
  • Sets priorities for the project team, ensures quality processes are followed, and collaboratively establishes and maintains deliverable timelines.
  • May provide performance related feedback to department managers for project staff.
  • Serves as the client's, investigators' and other stakeholders' primary point of contact for the project and/or assigned protocols.
  • Proactively addresses client's needs for ongoing studies/activities and engages with clients regarding new opportunities.
  • Develops, reviews, and approves project plans, study documents, and processes/SOPs, as needed.
  • Utilizes broad understanding of therapeutic, clinical trial design, and/or process expertise to influence and execute project decisions considering client needs, budget, scope, and the current state of the research field.
  • With input from team members, defines solutions that meet client's needs within project-defined scope.
  • Defines and approves approach or solutions to project requirements, risks and issues.
  • Communicates risks and contingencies to Emmes' project PI/Coordinating Center leaders, client, and/or internal Government Delivery oversight, as appropriate.
  • May contribute to developing, maintaining, and acquiring approval of budgets and statement of work documents and subsequent modifications prior to distribution to clients, as well as approvals for
    invoices and subagreements.
  • Liaises with Emmes' project PI/Coordinating Center leaders, corporate leaders and other Emmes departments to ensure staff resources are continuously informed, trained and efficiently utilized within the project team to successfully execute the project scope.
  • May provide input or participate in Corporate meetings (e.g., project reviews), central status reporting and information solicitations with Executive leaders, as applicable.
  • Uses key performance metrics to successfully execute the project scope.
  • Mentors project staff and supports staff development.
  • Models Emmes culture of integrity, accountability, collaboration, innovation, and perseverance across internal and external teams .
  • Aids in continuous corporate knowledge expansion by participating in relevant (internal and external) meetings/trainings to provide information learned and best practices to project teams, functional/service groups, and corporate entities as applicable.
  • Promotes and implements relevant corporate initiatives as directed.
  • Leads or contributes to the development of operational strategy, budget, and proposal content for new business opportunities, as assigned.
  • Represents Emmes at proposal, business development meetings, conferences, or other meetings, as requested.

Qualifications

Education/Requirements

  • Bachelor's and 6 years of empirical knowledge of the key
  • accountabilities/duties/responsibilities for the position with a
    typical tenure of at least 1 year project management experience
    in a research environment. (Required)
  • Master's and 4 years of empirical knowledge of the key
    accountabilities/duties/responsibilities for the position with a
    typical tenure of at least 1 year project management experience
    in a research environment.(Preferred)
  • PhD and 1 year of empirical knowledge of the key
    accountabilities/duties/responsibilities for the position with a
    typical tenure of at least 1 year project management experience
    in a research environment. (Preferred)
  • Project Delivery Track Record: Demonstratable track record of successfully delivering complex/high-priority clinical trials or clinical research projects within the agreed time, quality, and budget.

  • Experience in federally-funded research is preferred.

  • Clinical Research Knowledge: Demonstrated working knowledge of the principles of clinical research management and operations.

  • Problem-Solving: Demonstrated strong problem-solving and analytical skills, combined with sound business and ethical judgment.

  • Communication: Excellent verbal and written communication skills for client, team, and scientific interactions.

  • Leadership & Teamwork: Ability to work proactively and effectively, with creative problem-solving and collaboration skills. Highly motivated with the ability to work independently and as part of a multi-disciplinary team. Ability to mentor and support project staff.

  • Project Management: Strong cross-functional project management and time management skills.

  • Therapeutic Expertise (Preferred): Broad understanding of a therapeutic area, clinical trial design, and/or process expertise to influence and execute project decisions.

Why work at Emmes?

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

  • Flexible Approved Time Off
  • Tuition Reimbursement
  • 401k Retirement Plan
  • Work From Home Anywhere in the US
  • Maternal/Paternal Leave
  • Casual Dress Code & Work Environment


CONNECT WITH US!

Follow us on Twitter - @EmmesCRO

Find us on LinkedIn - Emmes

The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.

#LI-Remote


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About Emmes

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

201 - 500 Employees

Headquarters location

Rockville, MD, US

Year founded

1977

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