Regulatory Writing Consultant
2 settimane fa
About MMS
MMS is a leading Contract Research Organization (CRO) supporting the pharmaceutical, biotech, and medical device industries with a proven approach to complex trial data and regulatory submission challenges. With a global presence and a 97% customer satisfaction rating, MMS has been recognized as a top CRO in Global Health & Pharma's international awards programs for three consecutive years.
Job Overview
We are seeking a highly skilled Senior Medical Writing Consultant to join our team. The ideal candidate will have strong industry experience, excellent writing skills, and expertise in regulatory submissions. As a key member of our team, you will critically evaluate and analyze medical literature, write and edit clinical development documents, and interact directly with clients to coordinate projects.
Responsibilities
- Critically evaluate and analyze medical literature to select primary resource materials
- Write and edit clinical development documents, including clinical protocols, investigator's brochures, and clinical study reports
- Interact directly with clients to coordinate projects and ensure timely completion
- Maintain a high level of customer satisfaction and provide excellent internal and external customer service
Requirements
- At least 3 years of experience in the pharmaceutical industry
- Strong industry regulatory writing and clinical medical writing experience
- Bachelor's, Master's, or Ph.D. in a scientific, medical, or clinical discipline
MMS offers a unique opportunity to work with a talented team of professionals and contribute to the success of our clients.
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