MD or DO - Plasma Center Medical Director

Kedrion Biopharma GmbH; Oklahoma; On-site; USD 150,000 - 200,000; Part time

Benefits offered by this job

Full medical, dental, and vision coverage

Life insurance and retirement savings plans

Paid time off and sick leave

Training programs and development opportunities

Employee discounts and wellness initiatives

Job summary

Kedrion Biopharma GmbH is seeking a part-time Center Medical Director for its plasma donation center in Oklahoma. Candidates must be licensed M.D. or D.O. and will oversee donor safety, regulatory compliance, and manage clinical staff. This role requires strong clinical judgment and a commitment to donor health.

The position involves approximately 10 hours per week and offers a comprehensive benefits package including health coverage and paid time off.

Qualifications

• Licensed Doctor of Medicine (M.D. or D.O.) from an accredited medical school.
• Currently licensed in the state of practice.
• CLIA certification required or willingness to complete certification prior to contract execution.

Responsibilities

• Oversee medical integrity of plasma donation center.
• Ensure donor safety and regulatory compliance.
• Supervise clinical staff and manage adverse events.

Skills

Clinical judgment

Communication skills

Understanding of donor health

Regulatory compliance knowledge

Education

Licensed Doctor of Medicine (M.D. or D.O.)

Tools

CLIA certification

Job description

MD or DO – Plasma Center Medical Director

KEDPLASMA is a subsidiary of Kedrion Biopharma Inc., specializing in the collection and procurement of high‑quality plasma that is processed into plasma‑based therapies. Kedrion Biopharma Inc. is an international company that collects and fractionates blood plasma to produce and distribute plasma‑derived therapeutic products used to treat and prevent serious diseases, including hemophilia, primary immune system deficiencies, and Rh‑sensitization.

Job Summary

Support large‑scale donor care with clinical precision and regulatory rigor

As the Center Medical Director, you will oversee the medical integrity of our plasma donation center. You’ll ensure donor safety, regulatory compliance, and clinical excellence while supporting the production of plasma‑derived therapies that save lives worldwide. You will use your independent medical judgment to guide donor eligibility, manage adverse events, and supervise clinical staff. This is a part‑time role; a licensed M.D. or D.O. would dedicate about 10 hours a week.

Primary Responsibilities

• Supervise and certify Physician Substitutes and review their performance in CLIA‑designated testing.
• Evaluate donor health and suitability through physical exams, lab reviews, and medical history assessments.
• Review and approve abnormal test results and determine donor eligibility for continued participation.
• Ensure compliance with FDA, CLIA, cGMP, EU GMP, OSHA, PPTA, and COLA regulations.
• Administer and oversee immunizations and monitor donor reactions.
• Provide consultation on donor medical emergencies and suitability, including on‑call availability.
• Liaise with external medical providers for donor referrals and follow‑up.
• Review and approve moderate‑complexity test procedures and quality control reports.
• Propose updates to SOPs and clinical practices to improve safety and compliance.
• Maintain presence during red cell immunization procedures and borderline donor evaluations.
• Educate staff on donor health protocols and ensure informed consent is properly administered.
• Monitor donor satisfaction and ensure a respectful, safe, and supportive donation experience.

Managerial Responsibilities

• Supervise and support clinical staff, including hiring, training, and performance evaluations.
• Communicate performance standards and coach staff to meet or exceed expectations.
• Promote staff retention through a positive and professional work environment.
• Address employee concerns and coordinate with HR and leadership as needed.

Qualifications

• Licensed Doctor of Medicine (M.D. or D.O.) from an accredited medical school.
• Currently licensed in the state of practice.
• Strong understanding of donor health, immunization protocols, and regulatory compliance.
• CLIA certification required or willingness to complete certification prior to contract execution.
• Excellent clinical judgment and communication skills.
• Ability to work in a regulated environment with exposure to bloodborne pathogens.
• Comfortable with light physical activity including standing, walking, and occasional lifting.

Employment eligibility verification will be required at the time of hire. This position does not offer visa sponsorship now or in the future.

Employee Benefits

Kedrion Biopharma Inc. provides a comprehensive benefits package to support your health, happiness, and future. Benefits include:

• Health & Wellness– Full medical, dental, and vision coverage
• Financial Security– Life insurance, AD&D, and retirement savings plans
• Work‑Life Balance– Paid time off, sick leave, and paid holidays
• Career Growth– Training programs and development opportunities
• Extra Perks– Employee discounts, wellness initiatives, and more

Kedrion Biopharma Inc. is committed to providing equal employment opportunities to all employees and applicants. Discrimination and harassment based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws is prohibited. This policy applies to all employment terms, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

For questions about employment eligibility or accommodations, contact the Talent Acquisition team at [e-mail].

Kedrion Biopharma Inc. participates in E‑Verify and provides the federal government with Form I‑9 information to confirm employment authorization.