Associate Clinical Scientist

0-2 years

$83,200 - $104,000 per year

Fremont

10 March 21, 2025

Job Description

Job Type: Hybrid Education: M.Sc./M.Pharm/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Clinical Scientist
Location: Redwood City, CA (Hybrid Role)
Type: W2 Contract
Salary Range: $40/hr - $50/hr ($83,200 - $104,000 per year)

Job Summary:
As an Associate Clinical Scientist, you will collaborate 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. This role may require up to 20% travel.

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 sources (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 consistency per protocol specifications and regulatory standards (e.g., CDISC and SDTM).
Audit Trails & Documentation: Maintain detailed data change and justification records, ensuring traceability and GCP compliance.
Program-Level Document Development: Contribute to clinical protocols, investigator brochures, study reports, abstracts, manuscripts, presentations, and other communications.
Quality Control Checks: Prepare and conduct QC checks of clinical data summaries for stakeholders.
Protocol Compliance: Monitor trial implementation to assess protocol conduct and individual subject safety issues.
Stakeholder Interaction: Collaborate with investigators, study sites, vendors, and committees to support clinical trial objectives and manage queries appropriately.
Literature Reviews: Conduct literature reviews as required.

Requirements and Qualifications:

Master’s degree or higher in a scientific discipline or related field.
Strong collaboration skills and the ability to thrive in a high-energy, team-driven environment.
Detail-oriented with the ability to prioritize tasks and work independently.
Strong organizational skills and the ability to interpret, analyze, and report trial/program-level data effectively.
Proficient with Microsoft Office (Excel, Word), Electronic Data Capture, and other custom web-based software.
Excellent written and verbal communication skills.
Ability to travel up to 20%.

Desired Skills and Experience:

Clinical Development, Oncology, Data Validation, Data Reconciliation, Query Management, Data Standardization, CDISC, SDTM, cGCP, Excel, Word, and Electronic Data Capture.

Additional Information:

Bayside Solutions, Inc. is not able to sponsor candidates at this time.
Candidates must qualify as W2 candidates.

CCPA Privacy Policy:
For more information, please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at www.baysidesolutions.com.

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Associate Clinical Scientist

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