Job Description

Principal Investigator - Permanent - Lincoln, NE

Proclinical 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

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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