Center Medical Director

Join Parachute; Ruston (LA); On-site; USD 170,478 - 242,802; Part time

Job summary

Join Parachute is seeking a Center Medical Director in Ruston, LA to lead medical and laboratory operations. The role involves ensuring compliance with regulations, overseeing staff training, and maintaining a quality-focused approach to laboratory testing. Candidates must have a Doctor of Medicine or Doctor of Osteopathic Medicine, relevant certifications, and experience in laboratory management. This position provides a unique opportunity to impact donor safety and operational quality in a supportive team environment.

Qualifications

• Minimum of one year directing or supervising laboratory testing, with a focus on quality and safety.
• Must possess a valid state-issued medical license in good standing.
• Board certifications as applicable to the role.

Responsibilities

• Lead and manage medical and laboratory operations with high standards of care.
• Provide training and empower medical staff for continuous learning.
• Ensure compliance with all relevant regulations for donor safety.

Skills

Medical Leadership

Laboratory Operations Management

Regulatory Compliance

Staff Training

Quality Assurance

Education

Doctor of Medicine or Doctor of Osteopathic Medicine

Certification in anatomic or clinical pathology

Job description

Center Medical Director

Department: Center Medical

Employment Type: Contract / Temp

Location: Ruston, LA

Compensation: $150.00 / hour

Description

Type: Contract

Work Week: 4‑6 hours a week

Hourly Rate: $150

As the Center Medical / Laboratory Director, you will provide medical guidance and support to the Physician Substitutes, while offering training as needed. This role is central to ensuring the Donor Center meets all regulatory requirements and operates smoothly. You’ll be the go‑to expert for both the Donor Center and the Company.

Key Responsibilities

Medical and Laboratory Leadership:

• Lead and manage the medical and laboratory operations, ensuring they are conducted with the highest standards of care and compliance.
• Serve as the primary contact for health departments and regulatory agencies, ensuring all procedures meet CLIA regulations.
• Monitor donor suitability, safety, and product quality, providing valuable insights to enhance operations.

Staff Training and Development:

• Empower and equip the medical staff with the necessary training and certifications, fostering a culture of continuous learning and excellence.
• Provide compassionate guidance during challenging donor reactions and support in confidential counseling for those with concerning test results.

Commitment to Quality:

• Establish and maintain a quality‑focused approach to laboratory testing, ensuring accuracy and reliability in every aspect.
• Regularly review quality assurance reports and test results, ensuring that all procedures are followed meticulously.
• Create a safe and supportive laboratory environment, ensuring it meets all physical and environmental standards.

Regulatory and Safety Assurance:

• Ensure compliance with all relevant regulations, including 21 CFR 630.3(i) and 21 CFR 630.5, safeguarding both donors and staff.
• Manage donor counseling, testing, and follow‑up care with a focus on safety and well‑being.

Collaborative Communication:

• Offer constructive feedback to Center Operations Management and the Quality Assurance team, working together to continually improve processes.
• Participate in senior leadership meetings, contributing your expertise to help guide the Center’s success.

Qualifications

• Doctor of Medicine or Doctor of Osteopathic Medicine with the appropriate state licenses.
• Certification in anatomic or clinical pathology is ideal, though equivalent qualifications will be considered.
• A minimum of one year directing or supervising laboratory testing, with a focus on quality and safety, or 20 continuing medical education credits or equivalent laboratory training.
• A valid state‑issued medical license in good standing is required.
• Board certifications as applicable to the role.

Work Environment

• You will occasionally be involved in more hands‑on activities, including lifting or moving.
• This role involves frequent use of hands, fingers, and wrists, with some exposure to hazardous chemicals and bloodborne pathogens.
• Personal Protective Equipment (PPE) will be provided and required for specific tasks or areas.

In this role, you’ll have the opportunity to make a meaningful impact on both the safety of our donors and the quality of our operations, all while working within a supportive and collaborative team environment.