Senior Clinical Trial Associate

About the Role:

• This role supports clinical trial planning, coordination, and oversight.
• You will independently manage assigned study activities and operational workstreams.

Key Responsibilities:

• Maintain TMF and investigator site files, tracking study timelines and deliverables.
• Manage vendors, CTMS activities, and budget activities.
• Collaborate with sites, CROs, and cross-functional teams.

Qualifications:

• Bachelor's degree with 5+ years of relevant clinical operations experience.
• Solid understanding of GCP and applicable regulatory requirements.
• Strong organizational, communication, and problem-solving skills.

Benefits:

• Unlimited PTO, wellness perks, and virtual medical support.
• Health, dental, and vision insurance.