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Senior Manager, Clinical Scientist – Hematology
Job in
Edison, Middlesex County, New Jersey, 08818, USA
Listed on 2026-09-12
Listing for:
Jobtailor
Full Time
position Listed on 2026-09-12
Job specializations:
-
Healthcare
Clinical Research, Medical Science
Job Description & How to Apply Below
- Lead clinical study design, execution, and data interpretation across a full development program
- Partner with Medical Directors and cross-functional teams to shape study strategy and scientific direction
- Author and review protocols, amendments, clinical study reports, and other key clinical documents
- Drive medical and safety data review throughout the trial lifecycle to protect patient safety
- Apply therapeutic area knowledge to inform study design and risk mitigation
- Represent Clinical Sciences in scientific advisory boards, steering committees, and safety monitoring meetings
- Mentor and guide junior team members
- Ensure compliance with FDA, EMEA, ICH, and GCP standards across study activities
- Bachelor's degree required
- Advanced degree (PhD/MD/PharmD/MSc) in life sciences or healthcare preferred
- 8+ years of pharmaceutical clinical drug development experience
- Experience in rare hematologic conditions and/or immunologic diseases preferred
- Demonstrated knowledge of GCP, clinical study design, and clinical research methodology
- Proven track record driving clinical trial process improvements
- Strong scientific and analytical skills
- Compliance with FDA, EMEA, ICH, and GCP standards across study activities
- Right to work and educational qualifications may be verified through background checks
Demonstrates expertise in clinical study design, execution, and data interpretation, with a strong focus on compliance with FDA, EMEA, ICH, and GCP standards. Proven ability to mentor junior team members and drive clinical trial process improvements in the pharmaceutical industry.
Highest-signal resume keywords- Clinical Study Design
- GCP Compliance
- Clinical Research Methodology
- Pharmaceutical Clinical Drug Development
- Mentoring Junior Team Members
- Data Interpretation
- Protocol Authoring
- Clinical Study Report Review
- Risk Mitigation
- Scientific Advisory Board Representation
- Trial Lifecycle Management
- Process Improvement
- Therapeutic Area Knowledge
- Analytical Skills
- Patient Safety
- Collaboration
- Leadership
- Communication
- Bachelor's Degree
- Advanced Degree (PhD/MD/PharmD/MSc) Preferred
- FDA
- EMEA
- ICH
- GCP
- Rare Hematologic Conditions
- Immunologic Diseases
Position Requirements
10+ Years
work experience
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