Clinical Scientist / Sr. Clinical Scientist

Redwood City, CA 94065

Posted: 07/10/2019 Employment Type: Direct Hire Industry: Clinical & Scientific Job Number: 16031

Clinical Scientist / Sr. Clinical Scientist

Redwood City, CA

 

Responsibilities
  • Manage medical monitoring plans, site interactions, and reviewing data output from ongoing clinical studies and safety reviews
  • May be responsible for analytical support of clinical trial data (safety and efficacy), including gathering, analyzing, reviewing, interpreting, and providing preliminary assessments and recommendations
  • Analyze information to assess issues relating to protocol conduct and/or individual subject safety
  • Assist in communicating a clear overview of ongoing trial results to both internal (e.g., Board of Directors) and external stakeholders
  • Provide organizational support for Data Monitoring Committees and other applicable data review committees, including operationalizing the charter, preparing updates and data reviews, execution of meetings and adjudications, and communication of synthesized data reports
  • Support of clinical trial objectives; responds to or triages questions for appropriate escalation
  • Contribute to the organization, preparation, and execution of investigator and advisory board meetings in collaboration with the study team and external collaborators
  • Collaborate on the preparation of scientific material for conference presentations or publications

 

Qualifications:
  • Minimum of Master’ s Degree (PharmD/PhD, Masters, Nursing preferred) in life sciences. 5yrs minimum of Clinical Scientist industry experience
  • Prior experience in early-stage clinical research in the biopharmaceutical industry, Phase 1/2 oncology experience preferred
  • Experience in analysis and interpretation of clinical data (safety and efficacy); working knowledge of biostatistics, Good Clinical Practices, ICH, and other regulatory requirements for clinical studies
  • Experience working with clinical trial sites, including global clinical research experience
  • Ability to make independent, timely, and clinically appropriate decisions
  • Able to communicate (written and orally) clinical and scientific data to a variety of audiences
  • High level of organizational and project management skills
  • Ability to handle multiple projects at a time and have a strong attention to detail while understanding the higher-level strategy

 

Felicia Id-Deen

Apply Online

Send an email reminder to:

Share This Job:

Related Jobs: