Biotech Clinical Trial Manager: Lead Startup Studies

cAMPfield Therapeutics; Boston (MA); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Foundational role in biotech start-up

Collaborative, science-driven culture

Shape office environment

Job summary

cAMPfield is seeking a Clinical Trial Manager (aCTM) to drive day-to-day operations of clinical studies from startup to closeout. The role oversees CROs, vendors, timelines, budgets, and inspection-ready execution in a fast-paced biotech setting.

Ideal candidates have 5+ years in clinical operations with direct CTM ownership, strong ICH-GCP knowledge, and proven cross-functional leadership in small biotech environments.

Qualifications

• Bachelor’s in life sciences or related field; advanced degree preferred.
• 5+ years of clinical operations experience with CTM ownership.
• Strong knowledge of ICH-GCP, trial processes, and vendor oversight.

Responsibilities

• Support startup through closeout across studies; manage CROs and vendors.
• Develop study plans, protocols, ICFs, training materials.
• Ensure studies follow ICH-GCP and regulatory requirements.
• Lead cross-functional study team meetings; coordinate with various functions.
• Oversee data management, TMF completeness, and study closeout activities.

Skills

Clinical operations

CTM ownership

Vendor oversight

ICH-GCP

Cross-functional leadership

Education

Bachelor’s degree in life sciences

Advanced degree preferred

Job description

cAMPfield is seeking a Clinical Trial Manager (aCTM) to drive day-to-day operations of clinical studies from startup to closeout. The role oversees CROs, vendors, timelines, budgets, and inspection-ready execution in a fast-paced biotech setting.

Ideal candidates have 5+ years in clinical operations with direct CTM ownership, strong ICH-GCP knowledge, and proven cross-functional leadership in small biotech environments.