Senior Clinical Trial Associate — Drive Study Ops & Vendor Partnerships

Scorpion Therapeutics

Cambridge (MA)

On-site

USD 110,000 - 115,000

Full time

14 days+
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Benefits offered by this job

Equity
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Benefits

Job summary

Scorpion Therapeutics in Cambridge, MA is seeking a Senior Clinical Trial Associate to provide administrative and operational support across in-house and outsourced trials. You will help with start-up, maintenance, and closeout activities, while coordinating with CROs, vendors, and investigator sites.

The role requires a Bachelors degree and several years in clinical trials, with preference for FDA/EMA regulatory knowledge and ICH/GCP familiarity.

Qualifications

  • Bachelors degree required.
  • Minimum 3 years related industry experience required; Senior CTA requires 2 years as Clinical Trial Associate.
  • Familiarity with FDA/EMA regulatory requirements and ICH/GCP guidelines preferred.
  • Working knowledge of clinical protocols.
  • Proficiency with Microsoft Word, Excel, PowerPoint, Outlook.
  • Experience leading small group meetings and/or managing vendor relationships.

Responsibilities

  • Provide administrative and operational support across all study activities for in-house and outsourced trials.
  • Support study start-up, maintenance, and closeout activities.
  • Manage study-related vendors; serve as point of contact for CROs, contract labs, and other vendors.
  • Act as key point of contact for investigator sites to coordinate study-related activities.
  • Oversee sample collection, shipment, and analyses.
  • Reconcile and track study processes; identify risks and proactively resolve issues with CROs.
  • Assist with vendor management plans and compile study/quality metrics for CTL and review meetings.
  • Maintain documentation and correspondence with vendors and sites.
  • Ensure receipt, completeness, accuracy, and appropriate filing (TMF, SharePoint, and other systems) of clinical/administrative documents.
  • Support central IRB submissions and review site-specific informed consent forms.
  • Coordinate electronic distribution and/or shipment of study materials.
  • Track vendor and site contracts, budgets, invoices, and payments.
  • Contribute to TMF plan; perform periodic QC reviews and TMF reconciliation.
  • Perform study/department administrative tasks (agendas, minutes, meeting planning/presentations)

Skills

Communication
Organization
Detail-oriented
Teamwork
Verbal communication

Education

Bachelors degree

Tools

Microsoft Word
Microsoft Excel
PowerPoint
Outlook

Job description

Scorpion Therapeutics in Cambridge, MA is seeking a Senior Clinical Trial Associate to provide administrative and operational support across in-house and outsourced trials. You will help with start-up, maintenance, and closeout activities, while coordinating with CROs, vendors, and investigator sites.

The role requires a Bachelors degree and several years in clinical trials, with preference for FDA/EMA regulatory knowledge and ICH/GCP familiarity.

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