EPM Scientific are currently partnered with Biotech with an exciting & diverse pipeline. They are urgently seeking a Clinical Scientist to support their expanding clinical development team. See a short summary below:
Role Overview:
• Ideal Start Date: December, Flexible
• Location: New Jersey, Remote
• Contract Type: 6-Month Contract, Full Time
• Language: English
• Project: Oncology
Key Responsibilities:
• *
Act as a key clinical scientist supporting data review activities, with a focus on safety, efficacy, and timely delivery of critical data within the clinical trial team.
• Contribute to the development of study protocols and related documents (e.g., informed consent forms, amendments) and work with Clinical Operations to ensure delivery of essential study milestones.
• Provide scientific guidance and mentorship to junior clinical scientists, with potential to advance into a lead role and support scientific growth initiatives.
• Assist in generating, analyzing, and presenting clinical data for manuscripts, abstracts, and presentations, including authoring documents and preparing slides as needed.
• Promote consistency in medical and clinical data review techniques and standards across studies and programs.
Requirements:
• PhD, Pharm D, or RN degree is preferred.
• Strong experience (5+ years Preferred) in the drug development space.
• Strong understanding of clinical trial design, ICH-GCP, and regulatory requirements.
• Excellent analytical, communication, and organizational skills.
• Ability to work independently and manage multiple priorities in a fast-paced environment.
• Oncology Experience preferred.
If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.
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