Remotely
gcpregulatory complianceclinical trialsclinical developmentcrodata monitoringstudy protocolstranslational strategies
Job Description
📋 Description
- Oversees direction, planning, and interpretation of clinical trials in hematology, solid tumors, or
- Leads design/implementation of clinical development programs.
- Monitors study integrity and data for safety and efficacy.
- Oversees enrollment timelines and key deliverables with Clinical Ops.
- Develops protocols, CSRs, and regulatory submissions.
🎯 Requirements
- Bachelors in sciences; advanced degree preferred.
- 5+ years in clinical trials within pharma or academia.
- Ability to lead cross-functional global teams.
- Knowledge of trial methodology, regulatory standards, GMP/GCP.
- Strong English communication skills.
🎁 Benefits
- Competitive benefits package including PTO and medical/dental/vision.
- 401(k) eligibility and long-term incentive programs.
- Equal opportunity employer; supporting accommodation where applicable.
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