Job Details

Salary Range : $83,200 - $104,000 per year

Location : Redwood City, CA - Hybrid Role

Job Summary :

As an Associate Clinical Scientist, you will work with cross-functional teams and senior-level scientists to design, execute, and monitor multiple clinical studies. You will be responsible for discrete data review, interpretation, and communication tasks to internal and external stakeholders. Oncology and early-stage development experience is highly preferred. You may be required to travel up to 20% of the role.

Duties and Responsibilities :

• Data validation: Check data against predefined criteria and validation rules to identify discrepancies, errors, and missing values.
• Data reconciliation: Compare data across different sources, including CRFs, lab data, and eligibility packets, to ensure consistency and accuracy.
• Query management: Generate and resolve queries to clarify or correct data discrepancies.
• Data standardization: Ensure data is formatted consistently according to protocol specifications and regulatory standards (e.g., CDISC and SDTM).
• Audit trails and documentation: Maintain detailed data changes and justification records, ensuring traceability and GCP compliance.
• Contribute to developing program-level documents, including clinical protocols, investigator's brochures, clinical study reports, abstracts and manuscripts, presentations, and other internal and external documents and communications as needed.
• Prepare and conduct quality control checks of summaries of clinical data to internal and external stakeholders.
• Ensure trial implementation follows protocol and analyze information to assess protocol conduct or individual subject safety issues.
• Interact with internal and external stakeholders, including investigators, study sites, vendors, and committees, to support clinical trial objectives; respond to or triage questions for appropriate escalation.
• Conduct literature reviews as needed.

Requirements and Qualifications :

• Master's degree or higher in a scientific discipline or other relevant advanced degree in a health science field.
• 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, including Excel and Word), Electronic Data Capture, and other custom web-based software.
• Excellent written and verbal communication skills.
• Able to travel up to 20%.

Desired Skills and Experience:

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