Clinical Development Scientist

Bayside Solutions; California; Remote; USD 104,000 - 125,000; Full time

Job summary

An innovative firm is seeking a Clinical Development Scientist to join their dynamic team. In this pivotal role, you will be responsible for executing and monitoring clinical studies, ensuring data integrity, and collaborating with cross-functional teams. This position offers the opportunity to work on impactful clinical trials, utilizing your expertise in oncology and early-stage development. If you thrive in a fast-paced, collaborative environment and are passionate about advancing clinical research, this role is perfect for you. Join a forward-thinking company dedicated to innovation and excellence in the clinical development field.

Qualifications

• 4+ years of experience in clinical development required.
• Detail-oriented with strong organizational skills.

Responsibilities

• Validate and reconcile clinical data for accuracy.
• Interact with stakeholders to support clinical trial objectives.

Skills

Clinical Development

Data Review

Data Interpretation

Communication Skills

Organizational Skills

Education

Bachelor's Degree in Life Sciences

Advanced Clinical/Science Degrees (PhD, PharmD, MSN, MPH)

Tools

Microsoft Office

Electronic Data Capture

Medidata Rave

Job description

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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

$50.00/hr - $60.00/hr

Clinical Development Scientist

W2 Contract

Salary Range: $104,000 - $124,800 per year

Location: Redwood City, CA - Remote Role

Job Summary:

As a Clinical Development Scientist, you will work with the cross-functional teams and report to a senior-level or higher clinical scientist for the execution and monitoring of 1-3 clinical studies and be responsible for discrete tasks primarily regarding data review and interpretation, as well as communicating to both internal and external stakeholders in support of clinical trial objectives. Oncology and/or early-stage development experience is required.

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 (e.g., 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 trains 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/or conduct quality control checks of summaries of clinical data to internal and external 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.

Requirements and Qualifications:

• Bachelor's degree required; Life Sciences and Advanced Clinical/Science degrees are highly preferred (e.g., PharmD, PhD, MSN, MPH, etc.)
• Minimum 4+ years of experience in clinical development
• Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
• Proven ability to independently execute medical data review plan(s), secure database(s), and contribute to data interpretation and study reporting (CSR) collaboratively with other clinical development scientists/medical directors/cross-functional groups.
• 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 Microsoft Excel and Word), Electronic Data Capture, Medidata Rave, and other custom web-based software.
• Excellent written and verbal communication skills.

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.

Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at www.baysidesolutions.com.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Science

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