![]() ![]() The ideal candidate would hold a Ph.D.Must have at least 2 years of industry/ pharma or postdoctoral experience.Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary.Interact directly and independently with client to coordinate all facets of projects competent communicator skills for projects.Practice good internal and external customer service Overview 93 Reviews - Jobs 55 Salaries 14 Interviews 29 Benefits - Photos + Add a Review MMS Holdings Medical Writer Reviews Updated Find Reviews Clear All English Filter Found 11 of over 93 reviews Sort Popular Popular Highest Rating Lowest Rating Most Recent Oldest first 2.Maintain timelines and workflow of writing assignments.Complete writing assignments in a timely manner and have the ability to be flexible with changes in scope or timelines.Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, presentation materials and publications to medical journals, with initial guidance.Under initial supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.This role may require coming onsite from time to time. We offer competitive pay and a full benefits package. We are looking for candidates with at least 2 years of industry/ pharma or postdoctoral experience to join our team. For more information, visit or follow MMS on LinkedIn. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO in Global Health & Pharma’s international awards programs for the last three consecutive years. Updated Find Reviews Clear All Full-time, Part-time English Filter Found 85 of over 96 reviews Sort Popular Popular Most Recent Highest Rating Lowest Rating 3. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. MM S is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. ![]()
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