Lead Clinical Research Investigator

1 week ago


Los Angeles, United States ALLIANCE CLINICAL LLC Full time
Job Overview

We are in search of a distinguished and proficient Principal Investigator to oversee our clinical research initiatives. This role demands a comprehensive understanding of clinical trial management, ensuring adherence to established protocols, company standards, and Good Clinical Practice (GCP).

Key Responsibilities
  • Participant Safety: Guarantee the medical safety and well-being of all study participants.
  • Team Oversight: Supervise site personnel to ensure the execution of safe trial methodologies.
  • Data Review: Analyze and report on screening failures, safety metrics, and participant retention statistics.
  • Clinical Assessments: Manage the clinical evaluation processes associated with trial studies.
  • Regulatory Interaction: Maintain regular communication with Institutional Review Boards (IRBs) and study sponsors.
  • Compliance: Adhere to all medical responsibilities as outlined in study protocols, Standard Operating Procedures (SOP), GCP, and relevant state regulations.
  • Data Analysis: Collect and interpret data to identify trends and patterns within clinical trials.
  • Reporting: Prepare comprehensive reports detailing findings and recommendations for process enhancements.
  • Continuous Learning: Stay informed on the latest advancements in SOPs and documentation requirements.
Qualifications
  • Possession of an active and unrestricted Medical License in California.
  • A minimum of 2 years of experience as a Principal Investigator or Sub-Investigator is preferred, though we are open to training suitable candidates.
  • Demonstrated analytical capabilities with a strong aptitude for data collection, analysis, and interpretation.
  • Exceptional written and verbal communication skills for effective report writing and presentation of findings.
  • Proven ability to manage teams effectively and prioritize tasks in a dynamic environment.
  • Meticulous attention to detail and a commitment to maintaining confidentiality regarding sensitive information.

If you possess a strong motivation for clinical research and meet the qualifications outlined, we encourage you to consider this opportunity.

Job Type

Part-time

Compensation

Hourly Rate: $125.00 to $150.00

Expected Work Hours

5-20 hours per week

Education Requirement

Doctorate (Required)

License/Certification

California DEA Certification (Required)



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