Arvinas

Summer Intern – Clinical Operations

Arvinas

internship

Posted on:

Location Type: Hybrid

Location: New HavenConnecticutUnited States

Visit company website

Explore more

AI Apply
Apply

Job Level

About the role

  • Assist with study documentation and maintenance of trial master files (TMF)
  • Support coordination with study sites, CROs, and cross-functional teams
  • Help track study timelines and key deliverables
  • Perform basic data review and quality control checks for GCP compliance
  • Participate in team meetings and support operational reporting
  • Perform TMF filing, indexing, and quality control (QC) checks to ensure completeness and inspection readiness
  • Track TMF metrics and follow up on missing or incomplete documents
  • Support reconciliation activities (e.g., TMF vs. eTMF or vendor/CRO documents)
  • Help ensure documents are filed in accordance with GCP and internal SOPs

Requirements

  • Strong interest in clinical research; prior experience not required
  • Detail-oriented with good organizational skills
  • Strong communication and teamwork abilities
  • Proficiency in Microsoft Office
  • Eager to learn in a fast-paced environment
  • Arvinas will not be providing VISA sponsorship for this position now or in the future. You must have the ability to work without a need for current or future VISA sponsorship.
Benefits
  • group medical, vision and dental coverage
  • group and supplemental life insurance
  • competitive package of base and incentive compensation
  • comprehensive benefits program designed to support the health, wellness and financial security of our employees and their families
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
data reviewquality controlGCP complianceTMF filingindexingTMF metrics trackingreconciliation activities
Soft Skills
detail-orientedorganizational skillscommunication abilitiesteamworkeager to learn