Senior Clinical Trials Operations Lead

Regulatory Jobs; Boston (MA); On-site; USD 90,000 - 117,000; Full time

Benefits offered by this job

401(k)

Wellness programs

Discounts

Medical plans

Job summary

Centessa Pharmaceuticals is seeking a Sr. Clinical Trial Specialist to support trial planning and execution from a contract-to-hire basis. You will work with the CTM to ensure site start-up through close-out in compliance with SOPs, GCP, and regulatory guidelines.

Role emphasizes collaboration with study teams, budgeting, and documentation management, with potential conversion to a permanent position. Based in the US with occasional travel.

Qualifications

• BA/BS degree required.
• 4+ years in biotech or pharma.
• Experience with clinical sites and CROs is a plus.
• GCP knowledge.
• Proficient with Outlook, Word, Excel.
• Strong communication and problem-solving skills.
• Willingness to travel occasionally.

Responsibilities

• Support the CTM and study team in day-to-day trial operations.
• Prepare agendas, minutes, and materials for investigator and vendor meetings.
• Manage meeting logistics and travel arrangements.
• Track purchase orders, invoices, budgets, and payments.
• Monitor site initiation, activation, recruitment, and visit milestones.
• Maintain study tools for training, materials, and vendor access.
• Oversee vendor invoices and study documentation (ICF, protocols, TMF).
• Assist in data cleaning in preparation for database lock.
• Assist TMF management and up-to-date documentation upkeep.

Skills

Attention to detail

Communication skills

Problem-solving

Virtual work capability

Time-zone flexibility

Education

Bachelor's degree

Tools

Microsoft Office

Job description

Centessa Pharmaceuticals is seeking a Sr. Clinical Trial Specialist to support trial planning and execution from a contract-to-hire basis. You will work with the CTM to ensure site start-up through close-out in compliance with SOPs, GCP, and regulatory guidelines.

Role emphasizes collaboration with study teams, budgeting, and documentation management, with potential conversion to a permanent position. Based in the US with occasional travel.