Job Description

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.

Desired Skills and Experience

Clinical Development, Oncology, solid tumor, clinical trials, data analysis, Clinical Development Plan, Microsoft Office, Electronic Data Capture

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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