Job Description
Snelling Staffing is seeking a Principal Investigator. Will oversee all research projects and has overall accountability for the study. Following Good Clinical Practice (GCP) guidelines, the position will ensure that investigations are conducted according to the signed investigator statement, investigational plan, applicable regulations; for protecting the rights, safety, and welfare of subjects, and for the control of the investigational product under investigation. This position collaborates closely with Research Coordinators and Sub Investigators.
- Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with the FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
- Overall site leadership with focus on enhancing efficiencies, patient safety and protocol/GCP/regulatory compliance
- Evaluates and assesses participants to ensure only eligible participants enroll into the trials
- Report to the sponsor adverse experience that occur in the course of the investigation. Will read and understand the information in the IB, including the potential risks and side effects of the drug.
- Participates and engages in successful delivery and retention of study participants
- Interacts positively and collaboratively with sponsors, clients and team members
- Practices attention to detail in recording data and participant information, following protocol guidelines and GCP's
- Participate in Investigator Meetings (IMs) and continuing education activities in order to maintain current knowledge of recruitment affairs and issues
- Perform other dues as assigned.
Competencies: - Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities. Must possess a high degree of urgency, self-motivation, integrity and dependability. Ability to provide outstanding patient care. Ability to build rapport with patients and sponsors. Ability to work independently and to identify problems and implement solutions. Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
Requirements: - Minimum 3 years experience in clinical trials research or 10 years post training experience as a physician in general medicine or internal medicine
- Principal Investigator experience preferred
- Clinical skills in general medicine or internal medicine
- Clinical skills including phlebotomy, vitals, ECGs/EKGs, IVs, etc.
- Knowledge of clinical research operations, including Good Clinical Practice Guidelines
- Current Healthcare Provider BLS certification
- Excellent written and verbal communication skills
- Experience with MS Office
- High attention to detail
- Strong organizational and time management skills
This is a Direct Hire position! This company offers competitive pay based on experience and excellent benefits! For more information regarding this position, please email resumes to Karen Ramirez at [email protected] .
LOCATION Midland, Texas 79701
PAY $122 to $169 per hour
Job Tags
Hourly pay,