Kedrion Biopharma GmbH
Plasma Center Medical Director - Contractor, Part Time
Kedrion Biopharma GmbH, Las Vegas, Nevada, us, 89105
Plasma Center Medical Director - Contractor, Part Time
Overview
Plasma Center Medical Director - Contractor, Part Time
role at Kedrion Biopharma Inc. Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Kedrion Biopharma Inc. and its subsidiary Kedplasma are committed to providing equal employment opportunities to all employees and applicants, prohibiting 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 law. Position details: State/Province: Nevada | Job Location: Las Vegas | Place of Employment: Contract | Duration: Part Time Salary ranges are determined based on relevant experience, education, and certifications. If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at
kedtalent@kedrion.com . Employee Benefits
At Kedrion Biopharma Inc., we believe in taking care of our people. Our benefits package is designed to support your health, happiness, and future, including: 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 For specific inquiries please reach out to us. Job Summary
Support large-scale donor care with clinical precision and regulatory rigor As a
Center Medical Director , you will oversee the medical integrity of our plasma donation center. In this role, you’ll ensure donor safety, regulatory compliance, and clinical excellence while supporting the production of plasma-derived therapies that save lives worldwide. You’ll 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. What you'll do
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 and need-to-know
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. Kedrion Biopharma Inc. participates in E-Verify and provides Form I-9 information to confirm employment authorization. For more information, please contact the Department of Homeland Security.
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Plasma Center Medical Director - Contractor, Part Time
role at Kedrion Biopharma Inc. Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Kedrion Biopharma Inc. and its subsidiary Kedplasma are committed to providing equal employment opportunities to all employees and applicants, prohibiting 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 law. Position details: State/Province: Nevada | Job Location: Las Vegas | Place of Employment: Contract | Duration: Part Time Salary ranges are determined based on relevant experience, education, and certifications. If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at
kedtalent@kedrion.com . Employee Benefits
At Kedrion Biopharma Inc., we believe in taking care of our people. Our benefits package is designed to support your health, happiness, and future, including: 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 For specific inquiries please reach out to us. Job Summary
Support large-scale donor care with clinical precision and regulatory rigor As a
Center Medical Director , you will oversee the medical integrity of our plasma donation center. In this role, you’ll ensure donor safety, regulatory compliance, and clinical excellence while supporting the production of plasma-derived therapies that save lives worldwide. You’ll 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. What you'll do
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 and need-to-know
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. Kedrion Biopharma Inc. participates in E-Verify and provides Form I-9 information to confirm employment authorization. For more information, please contact the Department of Homeland Security.
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