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Contract Remote Clinical Trial Jobs (NOW HIRING)

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

Support the operational strategy related to assigned vendors, data flow, drug supply, remote ... Manages CRO and vendor budgets and invoicing procedures according to study contract * Summarizes ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... contract, budget, timelinesand withquality. Responsibilities As an expert in Clinical Trial ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... the trial contract, budget, timelines and with quality. Responsibilities As an expert in ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... contract, budget, timelines and with quality. Responsibilities As an expert in Clinical Trial ...

ICON

Clinical Trial Manager

Raleigh, NC · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Allen Spolden

Clinical Trial Associate

Manhattan, NY · Remote

$55K - $65K/yr

This is a remote position. This role offers the opportunity to support the planning and execution ... or contract research organization (CRO) industry. Requirements Candidates should possess an ...

Caribou Biosciences, Inc.

Clinical Trial Manager

Berkeley, CA · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We are seeking a Clinical Trial Manager (CTM) to join our Clinical Operations group. You will be ... This position may be onsite, hybrid, or remote. Responsibilities: Study Management * Manage ...

Caribou Biosciences, Inc.

Clinical Trial Manager

Berkeley, CA · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We are seeking a Clinical Trial Manager (CTM) to join our Clinical Operations group. You will be ... This position may be onsite, hybrid, or remote. Responsibilities: Study Management * Manage ...

4D Molecular Therapeutics

Associate Clinical Trial Manager

$34.25 - $46.75/hr

Track and route new CDAs, contracts and Work Orders through established legal approval process ... Basic knowledge of clinical trial operations, ICH GCP Guidelines and other applicable regulatory ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Perform clinical research site activities, which can include onsite or remote monitoring, co ... or implied contract between ARTBIO and the agency. ARTBIO will not pay any fees related to ...

CTI

Clinical Trial Manager

Covington, KY · Remote

Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ... May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre ...

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As of Aug 16, 2026, the average hourly pay for contract remote clinical trial 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.
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Infographic showing various Contract Remote Clinical Trial 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 $83,169 per year, or $40 per hour.

Senior Clinical Trial Associate (CONTRACT)

Entrada Therapeutics

Boston, MA • Remote

$36.50 - $49.75/hr

Contractor

Re-posted 12 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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