Clinical Trials Medical Writer

Description Job Title: Medical Writer Department: Study Set Up Location: Remote East Coast | Must Sit in East Coast Hours Per Week: 40 hours Schedule: Days, Monday - Friday SUMMARY The Medical Writer is responsible for interpreting complex clinical study protocols and other medical/scientific documentation to prepare and coordinate laboratory specification and study-specific medical/technical documents for ACM Global Laboratories. They will partner with internal departments in the development, drafting, review, editing, and finalization of documents used to conduct clinical studies. RESPONSIBILITIES Lead the development, revision, and maintenance of complex clinical study and amendments in accordance to standard operating procedures (SOPs) and regulatory requirements. With support of a mentor, work on the development, revision, and maintenance of high profile and expedited complex study documents and amendments in accordance to SOPs and regulatory requirements. Responsible for authoring and finalizing global lab specification documents (GLSD) and other related documents, as needed. Interpret, understand, and contribute to the scientific details of the protocol/technical documentation; identify and resolve gaps to ensure client satisfaction. Serve as a subject-matter expert (SME) for medical documentation utilized throughout the study lifecycle. Lead, initiate, and manage multiple rounds of internal and external document review. Liaise and drive timely collaboration between key stakeholders to ensure technical documentation meet high quality standards and aligns with business process. Participate in client interactions during study start-up activities and/or during study amendment process. Review of low to medium complexity GLSD in accordance to SOPs and Quality Assurance processes. With support of a mentor, work on the review of high complexity GLSD in accordance with SOPs and Quality Assurance processes. Lead the development, revision, and maintenance of lab manuals in accordance to SOPs and regulatory requirements. Review lab manuals to ensure alignment with SOPs and Quality Assurance processes. Resolve challenges and build consensus between all cross-functional groups and collaborators in a timely manner. Maintain a general working knowledge of Food & Drug Administration (FDA), Medical & Healthcare Regulatory Agency (MHRA), New York State Department of Health (NYSDOH), Good Clinical Practice (GCP), ICH and other pertinent regulations. Demonstrate initiative in professional self-development to improve job performance to maintain relevant working knowledge of clinical trials. Resolve queries for complex studies by using knowledge of regional differences and internal ACM processes for low and medium complexity GLSD and understanding of department responsibilities. Perform other duties and/or tasks as assigned. REQUIRED QUALIFICATIONS BA/BS, or equivalent experience in scientific field 1 yrs clinical trials or other laboratory experience required PREFERRED QUALIFICATIONS Applied knowledge of routine document content preparation, including the use of style guides, medical dictionaries, regulatory guidance documents, and templates Proficient in Microsoft Office and desktop publishing or word processing Education in medical or technical writing Excellent communication skills Ability to effectively influence others, work in a team environment, and collaborate across lines of business and functions 1+ years' experience drafting clinical trials documentation PHYSICAL REQUIREMENTS: Sedentary - Sedentary roles are primarily office-based and require prolonged sitting (67-100% of the workday) with minimal physical effort and lifting limited to under 10 lbs. Fine motor skills are necessary for computer work, writing, and telephone use, supported by clear visual and auditory ability. Cognitive and emotional demands are high due to extended concentration, frequent interruptions, independent decision-making, and information processi g. Altho