Principal Investigator - Permanent - Lincoln, NE
À±½·ÊÓƵ is seeking a dedicated Principal Investigator for a clinical research role in Lincoln, NE.
Primary Responsibilities:
The successful candidate will focus on overseeing clinical and administrative aspects of research projects within the analgesics and anaesthetics field. You will play a crucial role in ensuring the integrity and success of clinical trials.
Knowledge/Skills/Education/Licenses**
- MD or DO degree and current state license.
- Basic Life Support and Advanced Cardiac Life Support certification or willing to obtain upon hire.
- Successful completion of an ACGME residency program in family medicine, internal medicine, or emergency
- medicine.
- Ability to obtain DEA certificate for schedule II medications
- 3-5 years of medical/clinical experience preferred
- Clinical research experience preferred
The Principal Investigator's responsibilities will be:
Clinical:
- Oversee, reviews, and/or performs subject's medical history, as required
- Oversee and/or Conduct outpatient study procedures, as required by specific research project (skin assessments, etc)
- Oversee, reviews, and/or perform physical assessments, as required
- Records drug relationships for all Adverse Events
- Follow-up and/or close-out Adverse Events
- Oversee, review Pharmacy Custodian
- Review subject study charts for inclusion/exclusion
- Administer study drugs as assigned
Administrative:
- Review study protocol for feasibility of conducting study at CPMI
- Attends monitoring visits, study audits and all appropriate team meetings regarding study protocols
- Prepare for and participate in sponsor investigator meetings
- Assist associate administrators with Human Resources Operations, to ensure that personnel policies and regulations are met, and disciplinary actions are executed without coercion or bias judgment
- Assist associate administrators in the final Interview and in hiring decisions
- Oversee and review the documentation of subject's medical history and physical examination information
- Ensure the accurate maintenance of records with regards to the research project
- Administration of study drugs as required by the specific research project
- Supervise Pharmacy Custodian responsibilities
- Review adverse events, including serious adverse events for follow-up instructions and resolution
- Ensure that subordinates follow established guidelines in the collection of clinical data and/or administration of clinical studies
- Delegate authority at the site appropriately
- Discuss and administer Informed Consent Form
If you are having difficulty in applying or if you have any questions, please contact Damian Albera at d.albera@proclinical.com
À±½·ÊÓƵ is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
À±½·ÊÓƵ Staffing is an equal opportunity employer.
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