Sr. Clinical Trial Manager

Internetwork Expert

Boston (MA)

Hybrid

USD 125,000 - 170,000

Full time

8 days ago
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Benefits offered by this job

Health insurance
401k
Life Insurance
Paid time off
Family leave
Disability coverage
Training & development
Free food & snacks
Wellness resources
Stock options

Job summary

Frontier Medicines is seeking two Sr. 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 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.

Qualifications

  • Bachelor’s degree in a scientific/healthcare field or RN required.
  • 5–7 years of Clin Trial Manager or Clinical Project Management experience.
  • Experience supporting oncology studies preferred.
  • Vendor and CRO management experience.
  • Strong working knowledge of ICH-GCP guidelines.
  • Excellent organizational, problem-solving and time management skills.
  • Strong written and verbal communication with a collaborative approach.
  • Legally authorized to work in the United States.

Responsibilities

  • Support day-to-day activities within one or more trials: feasibility, site selection, start-up, maintenance, close-out.
  • Act as operational contact for CROs and trial sites, identifying and escalating issues.
  • Oversee CRO and vendor set-up, ensuring timely study initiation.
  • Review site regulatory documents and elevate to stakeholders as needed.
  • Ensure inspection readiness, TMF quality, and regulatory compliance.
  • Identify operational challenges and propose mitigation plans with senior team.
  • Review protocols, ICFs, CRFs and other documents as needed.
  • Monitor study performance metrics, timelines, CRO trip reports.
  • Track study budgets and vendor invoices, flag discrepancies.
  • Maintain timely study registration on ClinicalTrials.gov and registries.
  • Coordinate Clinical Trial Team meetings and action item follow-up.
  • Maintain trackers, databases, and repositories.
  • Provide regular study updates to stakeholders and support enrollment, database lock, and closeout.

Skills

Clinical Trial Management
Oncology trials experience
Vendor & CRO management
ICH-GCP knowledge
Organizational skills
Communication skills
Problem solving
Proactive attitude

Education

Bachelor’s degree in science/healthcare or RN

Job description

Frontier Medicines is seeking two Sr. 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 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.

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 elevate 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.
  • 5-7 years of Clinical Trial Manager/SCTM 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.
  • 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 $125,000 - $170,000. 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.

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