Job Description

Clinical Scientist (Manager/Senior Manager), Oncology

Location: New York, NY - This role is hybrid onsite. Candidates must be open to relocating to NYC or be able to commute into the city 2-3 times per week.

Scientific Search has recently partnered with a clinical-stage pharmaceutical company pioneering novel approaches to treating cancer. They’re looking for a Clinical Scientist, who will report to the Senior Director, Clinical Science and will work collaboratively with the clinical team to contribute to the development, evaluation and execution of oncology programs.

Responsibilities

• Collaborates closely with the Medical Monitor(s) to provide scientific input on planning, evaluation and analysis of clinical programs and trials
• Supports clinical data review and interpretation including subject eligibility review and monthly listing review
• Reviews emerging clinical data and supports identification of data trends and potential inconsistencies; raises appropriately to the clinical team.
• Supports safety monitoring activities and procedures to ensure patient safety and compliance with reporting requirements, including review of SAE narratives.
• Maintains data integrity and quality of clinical trial(s) in support of the development strategy for all assigned programs
• Collaborates with cross functional study team as appropriate to execute clinical study deliverables
• Assist with preparation/review of protocol and other study documents including medical monitoring plans, SAPs, informed consents, IBs, site training materials/presentations, and clinical components of the Clinical Study Reports and regulatory documents.
• Ensures compliance with FDA, GCP and other applicable guidelines as well as SOPs

Requirements

• Master’s Degree required, further advanced degree in related field preferred
• Minimum of 5 years of highly relevant experience related to conduct of clinical trials
• Experience in oncology required, experience in early phase trials preferred
• Strong working knowledge of FDA, ICH, GCP guidelines and other relevant regulatory requirements
• Experience working with EDC systems
• Strong analytical skills and attention to detail with the ability to work with large data sets and ensure consistency across the clinical study databases.

Base salary of approximately $115,000- $170,000 which may vary depending on qualifications, experience, and ultimate leveling.

How To Apply: We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to [email protected] and tell me why you’re interested. Or, feel free to email your resume.

Job Tags

Relocation,

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