ZipRecruiter

Log In

1

Contract Clinical Trial Assistant Jobs (NOW HIRING)

Actalent

Clinical Trial Manager- Hybrid

Cary, NC · Hybrid

Contract Clinical Study Manager Hybrid Raleigh-Durham (RTP) The Contract Clinical Study Manager ... risks. * Assist in vendor selection activities, including contributions to RFPs, scopes of work ...

New

Sagimet Biosciences

Clinical Trial Manager

San Mateo, CA · On-site

$90 - $100/hr

Job Type Contract Description The Clinical Trial Manager manages and leads the day-to-day clinical ... • Assist in the critical development and review of key study documents (e.g. Protocols, ICF ...

Actalent

Clinical Trial Manager- Hybrid

Raleigh, NC · Hybrid

Contract Clinical Study Manager Hybrid Raleigh-Durham (RTP) The Contract Clinical Study Manager ... risks. * Assist in vendor selection activities, including contributions to RFPs, scopes of work ...

Kura Oncology

Clinical Trial Associate

Boston, MA · On-site

$36.50 - $49.75/hr

Job Summary: The Clinical Trial Associate (CTA) supports the operational execution of clinical ... orders, contract setup, invoice processing, and tracking of study budgets. * Assist with ...

Icon plc

Clinical Trial Manager

Raleigh, NC · On-site

Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems * Ensure quality and completeness of TMF for assigned clinical trials * Participates in ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Manages CRO and vendor budgets and invoicing procedures according to study contract * Summarizes ...

Icon plc

Clinical Trial Manager

Houston, TX

Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems * Ensure quality and completeness of TMF for assigned clinical trials * Participates in ...

Clinovo

Clinical Trial Manager

Cambridge, MA · On-site

$175K/yr

CRO & Vendor Management * Act as the primary operational liaison for contract research ... Clinical Operations Leadership * Assist with management of study budgets, timelines, forecasting ...

New

ICON

Clinical Trial Manager

Raleigh, NC · On-site +1

Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems * Ensure quality and completeness of TMF for assigned clinical trials * Participates in ...

Icon plc

Clinical Trial Manager

Philadelphia, PA

Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems * Ensure quality and completeness of TMF for assigned clinical trials * Participates in ...

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

... orders, contracts, and amendments for sites/vendors. * Assist in developing study-specific ... Global Phase 3 clinical trial management experience * Minimum of 3 years of clinical trial ...

previous pagenext page

Showing results 21-40

All JobsContract Clinical Trial JobsContract Clinical Trial Assistant Jobs

Contract Clinical Trial Assistant information

See salary details

$11

$37

$68

How much do contract clinical trial assistant jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for contract clinical trial assistant in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What are some common challenges faced by contract clinical trial assistants, and how can they be managed effectively?

Contract Clinical Trial Assistants often juggle multiple studies and tight timelines, which can make prioritizing tasks and maintaining accuracy challenging. Effective organization, clear communication with study teams, and proactive follow-up on outstanding documents are essential for success. Since contract positions may involve working with various sponsors or CROs, adaptability and quick learning of new protocols and systems are also important. Building strong relationships with colleagues and staying updated on regulatory requirements can help manage these challenges and contribute to smooth trial operations.

What is a contract clinical trial assistant?

A Contract Clinical Trial Assistant (CTA) is a professional who provides administrative support to clinical research teams on a contractual basis. They help manage documents, organize trial-related materials, coordinate meetings, and ensure compliance with regulatory requirements. CTAs play a vital role in maintaining the accuracy and integrity of clinical trial data and often act as a liaison between different stakeholders. Contract CTAs are typically hired for specific projects or time periods, offering flexibility to both employers and employees.

What are the key skills and qualifications needed to thrive as a contract clinical trial assistant?

To thrive as a Contract Clinical Trial Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and Good Clinical Practice (GCP) guidelines is typically required. Excellent communication, time management, and problem-solving abilities help you collaborate effectively with cross-functional teams and manage multiple priorities. These skills and qualifications ensure accurate documentation, regulatory compliance, and efficient trial support in a fast-paced clinical research environment.

What is the difference between Contract Clinical Trial Assistant vs Clinical Trial Assistant?

AspectContract Clinical Trial AssistantClinical Trial Assistant
CredentialsTypically requires a relevant degree or certification in life sciences or healthcareSame as Contract CTA, often requiring similar qualifications
Work EnvironmentContract-based, often temporary assignments at pharmaceutical or biotech companiesPermanent or temporary roles within clinical research organizations or sponsors
Employer & Industry UsageUsed by CROs, pharma companies for project-specific needsCommon in clinical research settings, both permanent and contract roles
Search & Comparison IntentOften searched for contract roles, project-based workBroader search for clinical trial support roles

The main difference between a Contract Clinical Trial Assistant and a Clinical Trial Assistant lies in employment type and duration. Contract CTAs work on temporary, project-specific assignments, while Clinical Trial Assistants may hold permanent or longer-term positions. Both roles require similar qualifications and are integral to clinical research teams.

More about Contract Clinical Trial Assistant jobs
What cities are hiring for Contract Clinical Trial Assistant jobs? Cities with the most Contract Clinical Trial Assistant job openings:
What are the most commonly searched types of Contract Clinical Trial jobs? The most popular types of Contract Clinical Trial jobs are:
What states have the most Contract Clinical Trial Assistant jobs? States with the most job openings for Contract Clinical Trial Assistant jobs include:
What job categories do people searching Contract Clinical Trial Assistant jobs look for? The top searched job categories for Contract Clinical Trial Assistant jobs are:
Contract Clinical Trial Assistant jobs near you
Infographic showing various Contract Clinical Trial Assistant job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Senior Clinical Trial Associate (CONTRACT)

Entrada Therapeutics

Boston, MA • Remote

$36.50 - $49.75/hr

Contractor

Re-posted 9 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.

Apply