Nexagen Search is hiring a Principal Clinical Scientist (remote) for a late-stage biopharmaceutical company developing therapeutics for cancer. Nexagen Search is a life sciences focused recruitment firm and represents organizations in the biotechnology and pharmaceutical industries. To learn more about our company, please visit our website: www.nexagensearch.com

Summary

The Principal, Clinical Scientist will be an essential contributor to the scientific, clinical, and operational scope of clinical development programs with an emphasis on protocol-specific activities. The Principal Clinical Scientist will help drive the design, planning, and implementation of study protocols for assigned investigational products and will play a key role in supporting related regulatory activities. This role will work on cross-functional study management teams for the design, execution, and monitoring of clinical trials, as well as assist with data interpretation and communication to both internal and external stakeholders. This individual may also help support internal process improvement initiatives within the clinical department.

Responsibilities:

• Partner with cross-functional teams with potential oversight from senior team members to conduct clinical studies, including operational feasibility, data management deliverables, preparation of meeting materials, communication plans, safety and medical monitoring, data cleaning, preparation of status update reports, and study close-out activities.
• Support senior team members with medical monitoring reports, safety reviews, site interactions, and reviewing TFLs.
• May be responsible for analytical support of clinical trial data (safety and efficacy), including gathering, analyzing, reviewing, interpreting, and providing preliminary assessments and recommendations.
• Analyze information to assess issues relating to protocol conduct and/or individual subject safety.
• Assist in communicating a clear overview of trial results.
• Provide organizational support for Data Monitoring Committees, Safety Review Committees, or other applicable data review committees including operationalizing the charter, preparing updates and data reviews, execution of meetings and adjudications, and communication of synthesized data reports.
• Author protocols and contribute to authoring of clinical study reports, IBs, ICFs, training documents, and other clinical and regulatory documents.
• Interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalations.
• Act as recognized clinical expert for assigned studies both within and external to Arcus.
• Write and/or review collaborative abstracts, posters, and content for scientific meetings, conferences and publications.
• Support publication strategy execution including collaboration with investigators, KOLs, medical affairs and other internal/external stakeholders.
• Present at investigator meetings.
• Conduct literature reviews as needed.

 Qualifications:

• PhD degree in health science field, PharmD, MD or non-US equivalent, or other relevant advanced degree in a health science field.
• At least 5+ years of experience at a pharmaceutical, CRO or biotechnology company as a clinical scientist or related role.
• Experience in oncology or oncology immunotherapy clinical trials preferred.
• Experience with data analysis and interpretation as an understanding of safety and pharmacovigilance principles required.
• Ability to think strategically, innovatively, and tactically with an interest in clinical research and drug development.
• Demonstrated ability to evaluate, interpret and present complex scientific data (preclinical, clinical, translational) to inform scientific hypotheses and development strategy. Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies.
• Must be willing and possess the expertise to work effectively in a fast-paced, team-based matrix environment as well as the ability to function independently as appropriate. Flexible to accommodate changes in team and project needs.
• Ability to handle multiple projects at a time and have a strong attention to detail while understanding the higher-level strategy.
• Excellent interpersonal, verbal, and written communication skills.
• Ability to make independent, timely and appropriate decisions.

Compensation: the expected base salary for this position is $195-200k