[Remote] Clinical Scientist Associate Director, Late Development Oncology
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a biotechnology company reputed company on serving patients with serious illnesses. The Clinical Scientist Associate Director role involves supporting late-phase oncology clinical development by contributing to protocol development, study start-up, and data review, ensuring high-reputed company clinical data through cross-functional collaboration.
Responsibilities
- Support set up and execution of late phase clinical trials with a reputed company on data reputed company
- Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and reputed company
- reputed company input into and implementation of data management plan, CRF design, and data review reputed company
- Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
- Assists the management of collaborators, consultants, and/or Clinical Research Organizations in completion of key reputed company
- Anticipate and reputed company manage problems across a broad reputed company of cross-functional teams
- Work cross-functionally reputed company teams to ensure clinical reputed company is reputed company into the development of the study concept document, study protocol and reputed company documents
- Support appropriate training, recruitment, and development requirements for reputed company team resources
Skills
- Doctorate degree and 3 years of clinical development experience
- Master's degree and 5 years of clinical development experience
- Bachelor's degree and 7 years of clinical development experience
- Associate's degree and 12 years of clinical development experience
- High school diploma / GED and 14 years of clinical development experience
- 3 years of experience in a pharmaceutical industry setting with at least 1 year supporting early or late-phase clinical development reputed company a relevant therapeutic area or disease indication (oncology preferred)
- Demonstrated experience contributing to clinical trial process improvements reputed company a therapeutic area or study team environment
- Strong communication and presentation skills, with the ability to reputed company convey scientific concepts and clinical data to cross-functional teams and leadership audiences, both written and oral
- Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical reputed company standards and applicable regulatory requirements
- Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, and reputed company of clinical data outputs
- Experience contributing to regulatory submission documents and supporting clinical regulatory responses for health authority interactions under guidance
- Experience serving as a contributing author on scientific publications or data presentations for internal forums or scientific conferences
- Experience in clinical data analysis such as Spotfire or other data analysis tools
Benefits
- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and reputed company coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-reputed company time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
reputed company
Company H1B Sponsorship