Senior Clinical Trial Associate: Timelines & Quality

Deciphera Pharmaceuticals; Waltham (MA); On-site; USD 115,000 - 159,000; Full time

Benefits offered by this job

Competitive salary

Annual bonus

401(k) with company match

Parental leave

Job summary

Deciphera Pharmaceuticals is seeking a Senior Clinical Trial Associate (Sr. CTA) to support successful clinical studies within Clinical Operations.

You will partner with study leads and cross-functional teams to manage timelines, budgets, and quality throughout trials. The role requires 3+ years in clinical operations, strong knowledge of ICH/GCP, and the ability to independently manage trial components with minimal oversight.

Qualifications

• Bachelor’s or Master’s degree with 3+ years in clinical operations.
• Solid understanding of ICH/GCP and regulatory requirements.
• Ability to independently manage trial components with minimal oversight.

Responsibilities

• Coordinate study team meetings, draft agendas and minutes.
• Support site start-up activities and ongoing site management.
• Assist with TMF management, document filing and quality control.
• Maintain study trackers and systems to support execution.

Skills

Clinical operations

Attention to detail

Organizational skills

Project management

Communication skills

Education

Bachelor’s or Master’s degree

Tools

Clinical trial systems

Vendor platforms

Job description

Deciphera Pharmaceuticals is seeking a Senior Clinical Trial Associate (Sr. CTA) to support successful clinical studies within Clinical Operations.

You will partner with study leads and cross-functional teams to manage timelines, budgets, and quality throughout trials. The role requires 3+ years in clinical operations, strong knowledge of ICH/GCP, and the ability to independently manage trial components with minimal oversight.