Central Laboratory Scientist
1 week ago
Job Summary:
Responsibilities:
- Monitor laboratory operations in order to verify that accurate, precise, and reliable data are being generated for clinical trials;
- Interact with corporate leadership, administration, government agencies, accrediting agencies, and potential sponsors/clients to gain information and knowledge required to make appropriate business and/or operational recommendations and decisions;
- Ensure that accurate, precise, and reliable data are compliant with regulations, study requirements and Medpace SOPs and GCP
- Ability to troubleshoot technical issues;
- Ability to meet aggressive timelines;
- Routine flow cytometry data review and approval of clinical reports;
- Develop and conduct training within flow cytometry;
- Review and write Validation Plans/Reports/SOPs and;
- Oversee design, validation, and maintenance of flow cytometry assays in regulated environment
Qualifications:
- PhD in Laboratory Medicine, Immunology, Biochemistry/Biotechnology, Clinical Pathology or other similar area;
- Preferred, but not required, 2-3 years of experience in designing and conducting experiments using multi-color flow cytometry;
- Experience with analysis of flow cytometry data is required;
- Excellent communication and teamwork skills
- Excellent record keeping skills are required;
- Analytical Method Validation experience is preferred;
- Clinical research or translational research experience is preferred;
- Previous experience in a central lab environment is preferred; and
- Excellent interpersonal skills to effectively interact with and influence stakeholders, both internally and externally, are required.
Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 4,500 people across almost 40 countries.
Why Medpace?:
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package, flexible work arrangements (e.g., flex scheduling, remote working where applicable, etc.), and internal growth opportunities.
**Awards**:
- Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
- Recognized by Forbes as one of America's Best Mid-size Companies in 2021
- Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
**What to Expect Next**:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.
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