Principal Investigator – Clinical Research

Position Description

Odessa Research Institute is looking for a Physician (MD or DO) for a Principal Clinical Research Investigator position located in Odessa, Texas.

This is a unique opportunity for a medical professional to partner with an organization offering cutting-edge therapies and prophylaxes via coveted research projects with leading pharmaceutical and biotechnological companies. Join our dynamic team today as a part of groundbreaking research and make your mark in advancing medicine.

Ensures adherence to protocol requirements, protecting the rights and welfare of study subjects, assuring the integrity of data generated at the site. In executing these position responsibilities, the Investigator is guided by and promotes the adherence to FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Required Skills

• Act in a professional and caring manner towards patients, visitors, and colleagues, projecting a high quality and high service experience
• High ethical standards in line with company policies and procedures
• Self-starter able to plan and prioritize own workload
• Work collaboratively with colleagues to deliver services effectively and efficiently
• Attention to detail
• Safe handling of data and records regarding privacy and confidentiality, per HIPAA requirements
• Excellent communication skills
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.
• Must have knowledge of Microsoft Office Word, Microsoft Excel, Internet Explorer, Google Chrome, Mozilla Firefox, web-based enterprise solutions, and Electronic Case Report Form systems.
• Bilingual in Spanish is a plus.

Position Responsibilities

• Works with affiliate or collaborating research sites.
• Principal Investigator is the primary individual responsible for the preparation, conduct, and administration of all designated projects in compliance with applicable laws and regulations and institutional policies.
• Always maintains subject and document confidentiality and understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration, good clinical practice, International Conference on Harmonization, Health Insurance Portability and Accountability Act, Institutional Review Boards, and institutional policies and procedures.
• Performs study related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments. Reviews and adjudicates all lab, imaging, and biopsy findings.
• Reviews and holds expert knowledge of study related activities and protocols.
• Adheres to study protocols, Food and Drug Administration regulations, and good clinical practices at all times.
• Assists in the preparation for study monitor visits.
• Performs subject screening and recruitment.

Experience and Education

Certificates and License

• Current physician license
• Board Certified preferred
• Gastroenterology preferred specialty

Financial Benefits

• Competitive Salary.
• Profit Sharing.
• Paid Malpractice Insurance.
• Health Insurance.
• Paid Time Off.

Work Environment and Physical Demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Work is performed in an office/laboratory and/or a clinical environment.
• Exposure to biological fluids and/or bloodborne pathogens.
• Personal protective equipment required such as protective eyewear, garments, and gloves.
• Occasional travel may be required domestic and/or international.
• Ability to work in an upright and/or stationary position for 6-10 hours per day.
• Frequent mobility required.
• Occasional squatting, kneeling, or bending.
• Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.

Job Type: Full-time

Pay: $275,000.00 - $325,000.00 per year

Benefits:

• Health insurance
• Paid time off

Schedule:

• Monday to Friday

Supplemental pay types:

• Bonus pay

License/Certification:

• Medical License (Required)

Work Location: One location

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