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Entry Level Clinical Trial Associate Jobs (NOW HIRING)

REGENXBIO

In-House CRA / Clinical Trial Associate

Rockville, MD · On-site

$34.25 - $46.75/hr

As the In-house CRA you will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice ...

REGENXBIO

In-House CRA / Clinical Trial Associate

Rockville, MD · On-site

$34.25 - $46.75/hr

As the In-house CRA you will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice ...

Vanguard Clinical

Clinical Operations Associate (Pool)

CA · Remote

$70K - $80K/yr

We are experts in clinical trial operations with a focus on Clinical Trial Management, CRO/Vendor ... This is an exciting entry-level opportunity to join a fast-paced and dynamic learning environment ...

Solomon Page

Sr CTA - Autoimmune

San Diego, CA · On-site

$35 - $48/hr

The Senior Clinical Trial Associate supports the operational execution of clinical studies by partnering with internal Clinical Operations team, study sites, vendors, and CROs. This role is ...

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Entry Level Clinical Trial Associate information

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How much do entry level clinical trial associate jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for entry level clinical trial associate in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Clinical Trial Associate vs Clinical Research Coordinator?

AspectEntry Level Clinical Trial AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, often in life sciences; some certificationsBachelor's degree, often in health sciences; certifications preferred
Work EnvironmentClinical trial sites, pharmaceutical companies, CROsHospitals, clinics, research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, academic institutions, research organizations
Common Search & ComparisonYesYes

The Entry Level Clinical Trial Associate typically supports clinical trials by assisting with data collection, regulatory documentation, and trial logistics. The Clinical Research Coordinator often manages the overall conduct of clinical studies at research sites, including patient recruitment and compliance. While both roles require similar educational backgrounds and certifications, the Associate role is more focused on supporting trial activities, whereas the Coordinator oversees the entire study process at the site level.

What are the typical responsibilities of an entry level clinical trial associate?

As an Entry Level Clinical Trial Associate, your daily tasks often include maintaining clinical trial documentation, assisting with regulatory submissions, and supporting the coordination of study activities. You may also track trial progress, ensure data accuracy, and communicate with study sites to resolve issues or gather missing information. This role is highly collaborative, working closely with clinical research coordinators, project managers, and data management teams to ensure that trials run smoothly and adhere to protocols.

What is an entry level clinical trial associate?

Entry level clinical trial associates are professionals who support the planning, coordination, and administration of clinical trials, which are research studies conducted to test new medical treatments or drugs. They typically assist with tasks such as data entry, regulatory documentation, trial site communication, and ensuring compliance with study protocols. This role is ideal for individuals starting their careers in clinical research, offering valuable hands-on experience in the field. Entry level clinical trial associates often work under the supervision of clinical trial managers or coordinators and play a crucial role in the success of clinical studies.

What are the key skills and qualifications needed to thrive as an entry level clinical trial associate?

To thrive as an Entry Level Clinical Trial Associate, you need a bachelor's degree in life sciences or a related field, strong organizational skills, and attention to detail. Familiarity with clinical trial software (such as CTMS), regulatory documentation, and Good Clinical Practice (GCP) guidelines is important. Excellent communication, teamwork, and problem-solving abilities help you effectively support study coordination and interact with cross-functional teams. These skills and qualities ensure accuracy, regulatory compliance, and smooth execution of clinical research projects.
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Entry Level Clinical Trial Associate jobs near you
Infographic showing various Entry Level Clinical Trial Associate job openings in the United States as of August 2026, with employment types broken down into 72% Full Time, 14% Part Time, and 14% Contract. Highlights an 100% In-person job distribution, with an average salary of $83,169 per year, or $40 per hour.

Senior Clinical Trial Associate (CONTRACT)

Entrada Therapeutics

Boston, MA • Remote

$36.50 - $49.75/hr

Other

Re-posted 3 days ago

Job description

The Perfect Addition to Our Team

You are patient focused and excited about the opportunity to help support and develop the Clinical Operations organization at Entrada. You enjoy a fast-paced environment and juggling competing priorities. You follow up and follow through, connecting problems with solutions efficiently. You work successfully in a team environment with strong interpersonal skills to effectively build working relationships inside and outside the company. 

The Opportunity

This individual will assist the clinical operations team in the day-to-day operations, study start up and set-up, execution, and closeout of assigned trials.  The individual is accountable to the clinical trial team for the support of trial execution and works collaboratively with cross-functional team members and vendors to ensure proper set-up of trial processes and plans to execute the protocol in accordance with established SOPs and standards.

Responsibilities
  • Support the day-to-day operations of assigned trials to ensure completion per established project team goals and objectives in compliance with ICH/GCP guidelines, from study start-up to close-out.
  • Provides accurate and up-to date clinical trial information within relevant tracking tools and provides regular updates of trial progression to the clinical trial team, including those related to protocol deviations, adverse events, and site personnel trainings.
  • Contribute to the development of trial related plans and manuals.
  • Ensures timely maintenance of the TMF, filing and reconciliation according to regulatory guidance and internal SOPs.
  • Participates and ensures appropriate documentation of clinical team meetings, including meeting minutes, agendas, and action items.
  • Manage vendor POs and trial payments (including budget reconciliation), including invoice review and approval.
  • Support the set-up and management of clinical trial supplies and biosample management where needed (drug product, ancillary and other).
  • Assist in external training activities (suppliers, clinical sites etc.).
  • Assist in the management of trial completion activities, including data review, database lock and trial closeout.
The Necessities

At Entrada, our passion for science, our devotion to patients and our values drives our behavior:

  • Humanity - We genuinely care about patients and about one another.
  • Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.
  • Creativity - We are creative problem solvers.
  • Collaboration - We are more than the sum of our parts.
  • Curiosity - We have a growth mindset and push conventional thought and theory.

To thrive on our team, you will need to come with:

  • BA/BS degree with at least 2+ years of relevant experience in clinical operations working at a biotech or pharmaceutical company.
  • Strong understanding of clinical trial operations, including all phases from study start-up to close-out.
  • Ability to work independently and take initiative on projects under minimal supervision.
  • General working knowledge of drug development and ICH/GCP guidelines is required.
  • Previous CRO or vendor management experience preferred.
  • Excellent interpersonal, written, administrative, and computer skills.
  • Excellent verbal and written communication skills with a strong attention for detail.
  • Ability to travel approximately 5% of the time, as determined by the needs of the business. #LI-Remote #LI-JF1
  • This role is a long-term contract position that follows a remote working model, requiring monthly or quarterly travel to the Entrada Therapeutics Headquarters in Boston, MA.

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