Temp Clinical Scientist, Clinical Development

W2 Contract

Location: Redwood City, CA - Onsite Role

Job Summary:

As a Clinical Scientist, you will work with the cross-functional teams for the design, execution, and monitoring of clinical studies, as well as assist with data review, interpretation, and communication to both internal stakeholders. Oncology and/or late-stage experience is preferred.  Contribute to clinical development strategy and execution of the Clinical Development Plan (CDP).

Duties and Responsibilities:

• Partner with cross-functional teams with oversight from senior team members to conduct clinical studies, including study start-up, execution, close-out activities, database setup, data review/analysis, and preparation of study reports.
• Contribute to developing program-level documents, including but not limited to clinical protocols, investigator’s brochure, clinical study reports, abstracts and manuscripts, presentations, and various other internal and external documents and communications as needed.
• Conduct ongoing data reviews; prepare and present summaries to internal stakeholders.
• Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and/or individual subject safety.
• Interact with internal and external stakeholders (investigators, study sites, vendors, committees, etc.) to support clinical trial objectives; respond to or triage questions for appropriate escalation.
• Conduct literature reviews as needed.
• Travel: Up to 20%.

Requirements and Qualifications:

• BS/BA or master’s degree in a scientific discipline, or other relevant advanced degree in a health science field.
• Minimum 2 years of experience in the pharmaceutical or biotechnology industry as a clinical scientist or related role in oncology solid tumors.
• Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
• Detail-oriented with the ability to prioritize tasks and function independently as appropriate.
• Strong organizational skills and an ability to interpret, discuss, and report trial/program level data effectively and identify trends.
• Proficient with software tools (Microsoft Office), Electronic Data Capture, and other custom web-based software.
• Excellent written and verbal communication skills.

Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate.

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