Clinical Trial Associate

Deciphera Pharmaceuticals • Waltham, MA

1d • $90,000 - $124,000 • Onsite

About The Position

We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the execution of clinical studies within our Clinical Operations team. In this role, you will contribute to key trial activities and ensure that study components are delivered on time, within scope, and in compliance with quality and regulatory standards. You will work both independently and collaboratively, building your clinical operations expertise while partnering with experienced team members across cross-functional study teams.

Requirements

• Bachelor’s or Master’s degree with 1–3 years of experience in a pharmaceutical, biotech, CRO, or academic research setting
• Working knowledge of ICH guidelines, GCP, and global clinical trial regulations
• Ability to manage assigned study activities with guidance from senior team members
• Strong organizational skills and attention to detail

Nice To Haves

• Ability to quickly learn new tools, systems, and processes to improve efficiency
• Understanding of how clinical data, vendors, and systems interact across studies
• Strong written, verbal, and presentation skills
• A proactive, team-oriented mindset with the ability to work independently when needed

Responsibilities

• Coordinate cross-functional study team meetings, including preparing agendas and capturing meeting minutes
• Support site start-up activities and ongoing study coordination efforts
• Assist in managing external vendors as needed
• Participate in Investigator Meetings and contribute as appropriate
• Maintain and track essential study documentation, including regulatory documents such as 1572s in collaboration with Regulatory teams
• Support Trial Master File (TMF) activities, including document filing and quality control checks
• Assist with the creation, editing, and distribution of study materials (e.g., informed consent forms, manuals)
• Maintain study trackers, tools, and systems to support execution and compliance
• Support sample management activities and basic study logistics
• Contribute to the review and maintenance of study documents as needed
• Ensure assigned activities align with quality standards and regulatory requirements
• Collaborate with team members to identify when escalation or additional input is needed

Benefits

• Competitive salary and annual bonus.
• Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
• Generous parental leave and family planning benefits.
• Outstanding culture and opportunities for personal and professional growth.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level