Contract Clinical Trial Manager — Fast-Paced Biotech

Triveni Bio, Inc.; Watertown (MA); On-site; USD 96,000 - 105,000; Full time

Job summary

The Clinical Trial Manager role at Triveni Bio, Inc. oversees trials from start-up to close-out, ensuring GCP compliance and alignment with study budgets and timelines.

You will collaborate with cross-functional teams and manage vendor relationships to deliver high-quality data and patient safety across phase 1/2 studies. Based in a fast-paced biotech environment in Watertown, MA, you will lead site selection, feasibility assessments, and ongoing investigator coordination, while driving SOPs and

Qualifications

• Minimum 5 years of direct clinical trial experience with operations focus.
• Strong knowledge of GCP, ICH guidelines and regulatory requirements.
• Excellent problem-solving, communication and analytical skills.
• Experience in a fast-paced biotechnology environment preferred.
• Domestic and international travel up to 25%.

Responsibilities

• Manage clinical trials, timelines, scope, budget, quality and vendor oversight.
• Oversee feasibility and site selection processes, and build investigator/site relationships.
• Provide training and guidance to investigators and study teams.
• Ensure regulatory compliance, accurate documentation and SAE reporting.
• Collaborate with CROs and vendors to ensure deliverables meet requirements.
• Prepare regular trial status reports and assist in SOP development.
• Support study teams from feasibility through closeout.

Skills

Clinical trial management

GCP/ICH knowledge

Regulatory compliance

Vendor management

Site relationship management

Job description

The Clinical Trial Manager role at Triveni Bio, Inc. oversees trials from start-up to close-out, ensuring GCP compliance and alignment with study budgets and timelines.

You will collaborate with cross-functional teams and manage vendor relationships to deliver high-quality data and patient safety across phase 1/2 studies. Based in a fast-paced biotech environment in Watertown, MA, you will lead site selection, feasibility assessments, and ongoing investigator coordination, while driving SOPs and