Associate Clinical Scientist

Bayside Solutions; California; Hybrid; USD 83,200 - 104,000; Full time

Job summary

An established industry player is seeking an Associate Clinical Scientist to join their innovative team. In this role, you will collaborate with cross-functional teams to design and execute clinical studies, ensuring data integrity and compliance with regulatory standards. This position requires a Master's degree in a scientific discipline and offers the opportunity to thrive in a dynamic environment. You will engage with various stakeholders, manage data discrepancies, and contribute to essential clinical documentation. If you are detail-oriented and passionate about advancing healthcare through research, this role is perfect for you.

Qualifications

• Master's degree in a scientific discipline required.
• Strong communication and organizational skills are essential.

Responsibilities

• Conduct data validation and reconciliation for clinical studies.
• Prepare quality control checks and maintain compliance documentation.
• Interact with stakeholders to support clinical trial objectives.

Skills

Detail-oriented

Organizational skills

Excellent written and verbal communication

Ability to prioritize tasks

Education

Master's degree or higher in a scientific discipline

Tools

Microsoft Office

Electronic Data Capture

Custom web-based software

Job description

This range is provided by Bayside Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$40.00/hr - $50.00/hr

Associate Clinical Scientist

W2 Contract

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 brochure, 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.

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Seniority level

Mid-Senior level

Employment type

Contract

Job function

Research and Science