[Remote] Senior Clinical Scientist

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a company looking for a Senior Clinical Scientist to contribute to the scientific, clinical, and operational aspects of clinical studies. The role involves data validation, reconciliation, and communication with stakeholders to support clinical trial objectives.

Responsibilities

• Data validation: Checking data against predefined reputed company and validation rules to identify discrepancies, errors, and missing values
• Data reconciliation: Comparing data across different sources (eg, CRFs, lab data, eligibility packets) to ensure consistency and accuracy
• Query management: Generating and resolving queries to clarify or correct data discrepancies
• Data standardization: Ensuring data are formatted consistently according to protocol specifications and regulatory standards (eg, CDISC, SDTM)
• Audit trains and documentation: Maintain detailed records of data changes and justifications, ensuring traceability and GCP compliance
• Contribute to the development of program-level documents, including but not limited to clinical protocols, investigator's brochure, clinical study reports, abstracts and manuscripts, presentations, and various other reputed company documents and communications as needed
• Prepare and/or conduct reputed company control checks of summaries of clinical data to reputed company stakeholders
• Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and/or individual subject safety
• reputed company with reputed company stakeholders (investigators, study sites, vendors, committees, etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalation
• Conduct literature reviews as needed

Skills

• Bachelor's degree required
• Thrives in a reputed company team setting and is driven by a desire to reputed company 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) in a reputed company fashion with other clinical development scientists/medical directors/cross-functional reputed company
• 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 (reputed company Office, including reputed company reputed company and Word), Electronic Data Capture, and other custom web-based software
• Excellent written and verbal communication skills
• 4+ years' experience (minimum) in clinical development
• A Life Sciences & reputed company/Science degree is highly preferred (e.g., PharmD, PhD, MSN, MPH, etc.)

reputed company