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Entry Level Clinical Trial Associate Jobs (NOW HIRING)

Cellectis

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$100K - $130K/yr

Clinical Trial Associate Skyhawk Therapeutics is seeking a highly motivated CTA to provide administrative and operational support to Clinical Operations. Responsibilities : * Organize, participate in ...

New

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA

$100K - $130K/yr

Clinical Trial Associate Skyhawk Therapeutics is seeking a highly motivated CTA to provide administrative and operational support to Clinical Operations. Responsibilities : * Organize, participate in ...

New

Icon plc

Senior Clinical Trial Associate

Blue Bell, PA · On-site

$32 - $43.75/hr

Clinical Trial Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Sumitomopharma

Clinical Trial Associate

Marlborough, MA

$34.75 - $47.50/hr

Scope: The Clinical Trial Associate (CTA) plays a key role in supporting the operational and ... qualified entry-level candidates with relevant internship or academic project experience.

New

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research projects, working with the study team in the initiation, maintenance and closeout of clinical projects ...

Crinetics Pharmaceuticals

Clinical Trial Associate

$34.25 - $46.75/hr

The Clinical Trial Associate ("CTA") is a highly skilled specialist contributing to the development of relevant concepts, techniques and processes by assisting and helping lead the study team across ...

PTC Therapeutics

Contract, Clinical Trial Associate

Warren, NJ · On-site

$34.75 - $47.50/hr

The Contract, Clinical Trial Associate provides clinical study and Trial Master File (TMF) support for clinical operations. This involves supporting Clinical Trial Managers (CTMs) with activities ...

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All JobsEntry Level Clinical Trial Associate Jobs

Entry Level Clinical Trial Associate information

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

As of Jun 25, 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.

Can you be a CRA with no experience?

Becoming a Clinical Trial Associate (CTA) or similar entry-level role in clinical research typically requires some knowledge of Good Clinical Practice (GCP) and clinical trial processes, but prior experience is not always mandatory. Many employers offer training programs or onboarding to new hires, and relevant skills such as attention to detail, organization, and communication are valued. Starting in an entry-level position often involves gaining experience on the job and may lead to becoming a Clinical Research Associate (CRA) with additional training and experience.

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.

How to become a clinical trial assistant with no experience?

To become a clinical trial assistant with no experience, focus on gaining knowledge of clinical research processes through online courses or certifications such as the Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP). Entry-level roles often require strong organizational skills, attention to detail, and familiarity with electronic data capture systems; internships or volunteering can also provide relevant experience. Building a foundation in Good Clinical Practice (GCP) guidelines and developing basic computer skills can improve your chances of securing an entry-level position.

What are the typical responsibilities of an Entry Level Clinical Trial Associate on a daily basis?

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 are entry level clinical trial associates?

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.

How much does an entry level Clinical Research Associate make in the US?

An entry-level Clinical Research Associate in the US typically earns between $50,000 and $65,000 annually, depending on location, education, and certifications. Starting salaries may be lower but can increase with experience and additional training in clinical trial management and regulatory compliance.

Is a Clinical Research Associate entry level?

A Clinical Research Associate (CRA) is typically an experienced role that requires several years of industry experience and knowledge of Good Clinical Practice (GCP) guidelines. Entry-level positions in clinical research often include roles like Clinical Trial Assistant or Clinical Trial Coordinator, which may serve as stepping stones toward becoming a CRA.

What are the key skills and qualifications needed to thrive as an Entry Level Clinical Trial Associate, and why are they important?

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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What cities are hiring for Entry Level Clinical Trial Associate jobs? Cities with the most Entry Level Clinical Trial Associate job openings:
What are the most commonly searched types of Entry Level Clinical Trial jobs? The most popular types of Entry Level Clinical Trial jobs are:
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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 June 2026, with employment types broken down into 3% As Needed, 94% Full Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.
Clinical Trial Associate

Clinical Trial Associate

Repertoire Immune Medicines

Cambridge, MA • On-site

$36.50 - $49.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 26 days ago

Job description

Repertoire Immune Medicines is a clinical-stage biotechnology company harnessing the power of the human immune system to develop transformative therapies for cancer and autoimmune disease. Using its proprietary DECODETM platform—which maps the immune synapse between T cell receptors (TCRs) and their antigen targets—Repertoire translates unique biological insights into potent, targeted immune medicines. The company integrates deep protein engineering expertise and has established collaborations with several leading pharmaceutical companies, including Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer.
Repertoire is advancing a pipeline of TCR bispecific immunotherapies with the potential to address a broad range of cancers and autoimmune disorders. The company’s lead oncology program, RPTR-1-201, a TCR bispecific, is currently in a Phase 1/2 clinical trial across multiple solid tumor indications. Repertoire plans to advance additional TCR bispecific therapies into clinical trials over the next 12–18 months. The Clinical Trial Associate will play a central role in supporting these programs.Position SummaryRepertoire Immune Medicines is seeking a highly motivated Clinical Trial Associate (CTA) to join our Clinical Operations team and support the execution of early-phase oncology clinical trials. The CTA will provide critical operational support in execution of clinical trials across trial start-up, conduct, maintenance, and close-out activities. In this role, the CTA will work closely with the Director of Clinical Operations and the Clinical Trial Manager, cross-functional team members, CROs, vendors, and clinical sites to help ensure timely, high-quality operational execution of clinical trial activities in compliance with ICH-GCP, applicable FDA and global regulatory requirements, GDPR/HIPAA where relevant, and Repertoire SOPs.
The ideal candidate is detail-oriented, highly organized, proactive, and comfortable working in a fast-paced biotech sponsor environment, with experience supporting oncology and early-phase clinical trials preferred.
The successful candidate will also value a highly collaborative, in-person team culture and be expected to work on-site in our Cambridge office three or more days per week.Key Responsibilities
Clinical Trial Execution and Operational Support
  • Support operational full life cycle execution of early-phase oncology clinical trials in accordance with protocol requirements, ICH-GCP, applicable global regulations, and company SOPs.
  • Coordinate trial activities across multiple functional areas, CROs, vendors, and clinical sites to support timely execution of trial deliverables and milestones.
  • Identify operational issues, assess potential impact to trial timelines or compliance, and escalate risks or mitigation recommendations to Clinical Operations leadership as appropriate.
  • Support site activation, readiness for investigational product release, trial supply coordination, and issue resolution activities.
  • Maintain trial trackers, distribution lists, reports, and clinical systems.
  • Track trial progress, including key milestones, vendor deliverables, enrollment, monitoring activities, and trial action items.
Regulatory, Trial Master File (TMF), and Compliance Support
  • Manage, organize, and maintain trial documentation to support inspection readiness and perform TMF quality checks including identification and resolution of documentation gaps, inconsistencies, and compliance risks.
  • Support preparation, review, tracking, and maintenance of regulatory and IRB/IEC documentation in collaboration with internal and external stakeholders.
  • Support audit and inspection readiness activities, including document retrieval, issue tracking, and follow-up coordination.
  • Track protocol deviations, operational issues, and compliance concerns, including escalation of significant risks to trial leadership.
Cross-Functional Coordination and Trial Oversight
  • Serve as an operational contact for CROs, vendors, and clinical sites under the direction of Clinical Trial Manager.
  • Coordinate trial meetings, prepare agendas and minutes, document key decisions and action items, and support timely follow-up and resolution of operational priorities.
  • Support operational oversight of CRO and vendor deliverables, timelines, and issue escalation activities.
  • Coordinate exchange of trial information and materials across cross-functional stakeholders to support execution and inspection readiness.
  • Exercise independent judgment in prioritizing competing operational activities and managing multiple trial deliverables.
Qualifications
  • Bachelor’s degree in life sciences, health sciences, nursing, public health, or related field.
  • Minimum of 2 years of experience supporting clinical operations, clinical research, or clinical trial execution activities.
  • Working knowledge of ICH-GCP, FDA regulations, and clinical trial processes within a biotech, sponsor, CRO, or research environment.
  • Experience with clinical systems and tools such as eTMF, EDC, CTMS, Smartsheet, Box, and Microsoft Office applications.
  • Strong organizational, analytical, and problem-solving skills with demonstrated ability to prioritize competing activities and manage multiple deliverables.
  • Ability to identify operational risks, support issue resolution, and escalate quality or compliance concerns appropriately.
  • Strong communication and cross-functional collaboration skills with internal and external stakeholders.
  • Experience supporting oncology or early-phase clinical trials is preferred.
The base salary for this role ranges from $62,000 to $86,000 and is determined based on a candidate’s skills, experience, and internal equity. In addition to a competitive base salary, Repertoire offers a broad range of benefits designed to attract, retain, and motivate top talent, including medical, dental, vision, and life insurance, flexible time off, a 401(k) retirement plan, and short- and long-term incentive opportunities. Compensation and benefits are based on Repertoire’s good faith estimate at the time of publication and may be updated in the future.
 
Repertoire is committed to building an inclusive culture.  Much as the power of the immune system lies in the diversity of T and B cells, we believe our best work comes from a diverse workforce—and we are committed to pursuing that in all facets of the work experience.
Repertoire is proud to be an Equal Opportunity Employer.  

Recruitment & Staffing Agencies: Repertoire Immune Medicines (“Repertoire”) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Repertoire or its employees is strictly prohibited unless contacted directly by Repertoire’s internal Human Resources team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Repertoire, and Repertoire will not owe any referral or other fees with respect thereto.

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