Clinical Trial Manager Boston, MA

cAMPfield Therapeutics, Inc.; Boston, Northern (MA, KY); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Competitive compensation

Benefits package

Job summary

cAMPfield Therapeutics, Inc. in Boston is seeking a Clinical Trial Manager (CTM) to drive day-to-day management of clinical studies from startup through closeout.

You will oversee CROs, vendors, timelines, and budgets, ensuring inspection-ready execution across all phases of trials and maintaining high-quality TMF documentation. The ideal candidate has at least 5 years in clinical operations with CTM ownership, strong ICH-GCP knowledge, and a proven ability to lead cross-functional teams in a

Qualifications

• 5+ years of clinical operations with CTM ownership.
• Experience in biotech/pharma with ICH-GCP.
• Proven vendor oversight and site management.
• Strong communication and cross-functional leadership.

Responsibilities

• Oversee study planning, timelines, budgets, and CRO/vendor oversight.
• Ensure regulatory compliance and TMF quality.
• Lead cross-functional study team meetings.
• Support inspection readiness and audits.

Skills

CTM ownership

Cross-functional leadership

ICH-GCP knowledge

Vendor oversight

Biotech/pharma experience

Excellent communication

Education

Bachelor’s degree in life sciences

Advanced degree (MS/PhD) in life sciences

Job description

cAMPfield is a clinical-stage biopharmaceutical company focused on developingwell-tolerated and highly effective oral medicines, founded and led by industry veterans with success developing therapies for immune-mediated inflammatory diseases, includinginflammatory bowel disease (IBD).

About the Role

TheClinical Trial Manager (CTM)is responsible for supporting the day‑to‑day management of clinical studies from startup through closeout. This role is ideal for someone who is energized by cross‑functional collaboration, proactive problem‑solving, and the pace of an emerging biotech. The CTM will oversee CROs, vendors, timelines, budgets, and ensure inspection‑ready execution across all phases of the trial.

Key Responsibilities

Study Planning & Execution

• Support the overall operational planning, study startup, site selection, and activation activities under the direction of senior Clinical Operations leadership.
• Assist in the development and review of core study documents (protocols, ICFs, etc.) and drive the development of study plans, manuals, and training materials.
• Ensure studies are conducted in accordance with ICH‑GCP, regulatory requirements, and internal SOPs.
• Serve as the day‑to‑day operational contact for CROs and external vendors, supporting escalations to senior Clinical Operations leadership as appropriate.
• Oversee monitoring activities, enrollment performance, site engagement, and risk mitigation.
• Review vendor deliverables, KPIs, and quality metrics; elevate issues proactively.

Clinical Operations Leadership

• Assists with the overall management of study timelines, budgets, and forecasting; support contract and SOW development.
• Lead cross‑functional study team meetings and ensure alignment across Clinical Development, Biometrics, Safety, and Regulatory.
• Support inspection readiness and contribute to audit responses and CAPAs.

Data & Quality Oversight

• Partner with Data Management on database build, data cleaning, and query resolution.
• Review clinical data listings, safety narratives, and protocol deviations.
• Ensure high‑quality documentation and TMF completeness.

Study Closeout

• Oversee site closeout, reconciliation activities, and final study reporting.
• Contribute to CSR development and lessons‑learned processes.

Qualifications

• Bachelor’s degree in life sciences or related field; advanced degree preferred.
• 5+ years of clinical operations experience in biotech/pharma, with direct CTM‑level ownership of clinical studies.
• Strong understanding of ICH‑GCP, clinical trial processes, and vendor oversight.
• Experience working in small or emerging biotech environments strongly preferred.
• Ability to manage multiple priorities, anticipate issues, and comfortable operating with a high degree of autonomy as well as under the guidance of senior team members.
• Excellent communication, organization, and cross‑functional leadership skills.

What We Offer

• The opportunity to play a foundational role in a mission‑driven biotech start‑up.
• A collaborative, science‑driven culture where operational excellence is valued.
• The ability to shape the office environment and operational backbone of a growing company.
• Competitive compensation and benefits.

As set forth in cAMPfield Therapeutics, Inc.’s Equal Employment Opportunity policy,we do not discriminate on the basis of any protected group status under any applicable law.