AdresseJob Summary :
Awards:
EO/AA Employer M/F/Disability/Vets
Our corporate activities are growing rapidly, and we are currently seeking full-time, Experienced Regulatory Affairs Associate/ Specialist- Chemistry, Manufacturing, and Control (CMC). This person will work on a Regulatory Affairs project team to accomplish tasks and projects that are instrumental to the company’s success. With this opportunity, you will be able to leverage previous expertise and continue to develop and grow your career even further within the drug development industry
Responsibilities :- Support the development and execution of global CMC strategy in support of clinical trial activities and RA project team goals across multiple projects (pre-approval only);
- Support the writing, preparation, development, and review of CMC documentation including Investigational Medicinal Product Dossiers (IMPDs), Module 3 documents, and Quality Overall Summaries, as well as the CMC sections of other regulatory documents, including scientific advice briefing documents and Investigator’s Brochures;
- Provide CMC support and guidance to the Medpace project team and the Sponsor to support the scope of assigned projects;
- Maintain up-to-date knowledge and understanding of global regulatory CMC requirements, guidance, conventions, and technologies;
- Maintain timelines for CMC components of regulatory deliverables;
- Ensure all CMC documents and deliverables are completed within the agreed upon timelines and developed with full compliance to all regulatory guidance, internal review and quality control processes; and
- Support RA project teams and Sponsors in response to Regulatory Authority CMC queries and participate in meetings and teleconferences with Regulatory Agencies as needed. Ensure submissions comply with applicable regulations and guidance documents.
- Bachelor’s degree in a Health or Science field;
- At least 3 years of prior experience in the research or pharmaceutical industry;
- Experince with CMC development;
- Experience in supporting the development of CMC documents (IMPDs and Module 3) in support of global regulatory filings;
- Demonstrated experience supporting CMC project deliverables
- Strong computer skills, project management skills, and a high level of attention to detail;
- Demonstrated strong communication (both written and oral) and interpersonal skills to positively influence internal and external teams; and
- Ability to work independently with little to no guidance as well as demonstrate ability to act as a team player.
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 5,000 people across 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 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.
EO/AA Employer M/F/Disability/Vets
WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.
