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Full Time Clinical Trial Manager Jobs (NOW HIRING)

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

Frontier Medicines is seeking two Clinical Trial Managers to support the day-to-day execution of our oncology clinical trials as they advance through clinical development. Working under the guidance ...

Position Summary The Clinical Trial Manager (CTM) is responsible for the overall operational management and execution of clinical trials from initiation through close-out. This includes leading the ...

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

Frontier Medicines is seeking two Clinical Trial Managers to support the day-to-day execution of our oncology clinical trials as they advance through clinical development. Working under the guidance ...

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

We are seeking a Clinical Trial Manager with experience in managing a global Phase 3 clinical trial. Works with senior Clinical Operations members to lead the clinical project team members in the ...

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials including study start-up, site management and monitoring activities. This includes vendor management ...

Knowledge and experience in clinical study budgeting including timeline and the application of clinical trial performance metrics. Demonstrated ability to support the development and management of ...

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed

Senior Clinical Trial Manager Vancouver, WA (Onsite), Remote/Hybrid (US-based) We are seeking an experienced Senior Clinical Trial Manager to independently lead the end-to-end operational execution ...

New

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed

Clinical Trial Manager

Boston, MA · On-site

$133K - $150K/yr

The Clinical Trial Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. The ideal candidate will embrace a collaborative, innovative culture that ...

POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end execution of clinical trials, ensuring studies are delivered on time, within budget, and in compliance with ...

POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end execution of clinical trials, ensuring studies are delivered on time, within budget, and in compliance with ...

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Full Time Clinical Trial Manager information

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How much do full time clinical trial manager jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for full time clinical trial manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.
What cities are hiring for Full Time Clinical Trial Manager jobs? Cities with the most Full Time Clinical Trial Manager job openings:
What are the most commonly searched types of Clinical Trial Manager jobs? The most popular types of Clinical Trial Manager jobs are:

Clinical Trial Manager

Frontier Medicines

Boston, MA • On-site

$120K - $150K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago


Job description

Frontier Medicines is seeking two Clinical Trial Managers to support the day-to-day execution of our oncology clinical trials as they advance through clinical development. Working under the guidance of our Director/Sr. Director, Clinical Operations, you will serve as a key operational contact for our CROs and trial sites, helping drive feasibility assessments, site selection, start-up, maintenance, and close-out.

This is a great opportunity for someone who wants hands-on ownership of trial execution at a growing, clinical-stage biotech, with direct exposure to program strategy and cross-functional leadership. This is a hybrid role based in our Boston, MA office, with an expectation of 2-3 days per week onsite, plus periodic travel to trial sites and CRO/vendor meetings as needed.

Requirements

What will you be doing?

● Support day-to-day activities within one or more clinical trials, including country/site feasibility assessments, site selection, start-up, maintenance, and close-out.

● Serve as a key operational point of contact for CROs and trial sites, identifying and escalating potential issues as needed.

● Assist with oversight of CRO and vendor set-up, liaising with CROs to ensure timely study initiation.

● Review site-level regulatory documents (e.g., Informed Consent Forms, essential documents) and escalate to appropriate stakeholders as needed.

● Help ensure inspection readiness, TMF quality, and adherence to protocol and regulatory requirements.

● Proactively identify potential operational challenges and, in partnership with senior team members, propose mitigation plans to keep study execution on track.

● Assist with review of protocols, master template informed consent forms, case report forms, and other clinical study documents as needed.

● Monitor study performance metrics, timelines, and deliverables, and review CRO trip reports for trends and quality issues.

● Track study budgets and vendor invoices/change orders in partnership with Clinical Operations and Finance, flagging discrepancies as needed.

● Help maintain timely and accurate study registration and updates on ClinicalTrials.gov and other applicable registries.

● Coordinate Clinical Trial Team meetings and drive action item follow-up.

● Maintain clinical operations trackers, databases, and document repositories.

● Provide regular study updates to internal stakeholders and support enrollment, database lock, and study closeout activities.

Traits we believe make a strong candidate:

● Bachelor's degree in a scientific, healthcare, or related field, or an RN, required.

● 3-4 years of Clinical Trial Manager or Clinical Project Management experience, ideally supporting oncology clinical trials.

● Experience supporting oncology studies strongly preferred.

● Vendor and CRO management experience.

● Strong working knowledge of ICH-GCP guidelines and clinical trial regulations.

● Excellent organizational, problem-solving, and time management skills, with strong attention to detail.

● Strong written and verbal communication skills with a collaborative, team-oriented approach.

● Comfortable in a fast-paced, dynamic environment; a proactive, roll-up-your-sleeves mindset.

● Legally authorized to work in the United States.

Benefits

  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan (401k, IRA)
  • Life Insurance (Basic, Voluntary & AD&D)
  • Paid Time Off (Vacation, Sick & Public Holidays)
  • Family Leave (Maternity, Paternity)
  • Short Term & Long Term Disability
  • Training & Development
  • Free Food & Snacks
  • Wellness Resources
  • Stock Option Plan

At Frontier, we strive to build a diverse and equitable workplace. The salary range for this role is $120,000 - $150,000 Compensation for the role will depend on a number of factors, including candidates' qualifications, skills, competencies and experience. Frontier offers a competitive total rewards package which includes healthcare coverage, 401k and a broad range of other benefits.

This compensation and benefits information is based on Frontier's knowledge as of the date of publication, and may be modified in the future.