Senior Clinical Trial Manager — Early-Phase Immunology

ADP, Inc.

Watertown (MA)

On-site

USD 130,000 - 170,000

Full time

14 days+
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Job summary

Seismic Therapeutic in Watertown, MA seeks an experienced Clinical Trial Manager or Senior Clinical Trial Manager to drive operational planning and execution for early-phase studies under the Director of Clinical Operations.

You will manage study workstreams from start-up to closeout, coordinate CRO/vendor activities, maintain visibility, and escalate risks with recommended actions. Domestic and international travel may be required.

Qualifications

  • Bachelor’s degree in life sciences, nursing, pharmacy, or related field.
  • 5+ years (Clinical Trial Manager) or 8+ years (Senior) of clinical trial experience in Phase 1/2.
  • Experience coordinating CRO/vendor management; global trial experience a plus.
  • Working knowledge of ICH-GCP and regulatory requirements.
  • Proficiency with EDC, CTMS, eTMF; strong Microsoft Office skills.
  • Ability to travel domestically and internationally.

Responsibilities

  • Coordinate day-to-day operational activities for studies with CROs and vendors.
  • Develop and maintain study plans, risk logs, enrollment forecasts, and metrics.
  • Contribute to protocols, informed consent, eCRFs, and study procedures.
  • Oversee monitoring activities, data quality indicators, and site findings.
  • Maintain inspection-ready TMF documentation and sponsor oversight.
  • Coordinate cross-functional study activities and meetings; document actions.

Skills

CRO/Vendor Management
Global trial coordination
Risk escalation
ICH-GCP knowledge
Excellent communication

Education

Bachelor’s degree in life sciences, nursing, pharmacy, or related field
Advanced degree a plus

Tools

EDC
CTMS
eTMF
IRT/RTSM
Microsoft Excel
PowerPoint
Word

Job description

Seismic Therapeutic in Watertown, MA seeks an experienced Clinical Trial Manager or Senior Clinical Trial Manager to drive operational planning and execution for early-phase studies under the Director of Clinical Operations.

You will manage study workstreams from start-up to closeout, coordinate CRO/vendor activities, maintain visibility, and escalate risks with recommended actions. Domestic and international travel may be required.

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