Medical Writing Consultant or Regulatory Affairs Medical Writer -...
DivIHN Integration Inc - Atlanta, Georgia, United States
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For further inquiries regarding the following opportunity, please contact one of our Talent Specialist: Hema at
630 847 0275 Meghna at
224 369 4230
Title: Medical Writing Consultant or Regulatory Affairs Medical Writer - Remote (Part Time) Location: Remote Duration: 7 Months Estimated Hours per Week : 20
Job Description: As a Pharmaceutical Consultant, you will play a crucial role in providing medical writing direction and guidance for various projects. Your expertise will ensure that all documentation aligns with client's style guide and meets the necessary regulatory standards (US and EMA). You will be responsible for the following: Key Responsibilities: Provide medical writing direction and guidance aligned with client's style guide for assigned projects, including the review of work products. Convert relevant data and information into formats that comply with TM document requirements and coordinate the review of the final products. Understand, assimilate, and interpret various sources of information with appropriate guidance and direction from the TM team. Confirm the completeness and accuracy of information presented in documents. Perform literature searches as needed to gather relevant content for drafting documents. Maintain expert knowledge of US and international regulations, requirements, and guidance associated with scientific publications, including US FDA and ICH guidelines. Utilize prior knowledge of preclinical strategy, pharmacology, toxicology, and GLP practices to ensure that documents drafted at client are prepared for regulatory inspection or audit in the US or Europe. Complete draft reports based on data provided by client Subject Matter Experts (SMEs) to ensure thoroughness and compliance. Review draft training modules on GLP's, regulatory writing and FDA interactions and provide suggestions on ways to modernize. Qualifications: Advanced degree in Life Sciences, Pharmacy, or a related field. Proven experience in medical writing within the pharmaceutical or biotech industry. Regulatory Affairs Certification and/or PMP certification Strong understanding of regulatory requirements and guidance related to scientific publications. Excellent analytical skills and attention to detail. Ability to work collaboratively with cross-functional teams and communicate effectively. Proficient in conducting literature searches and synthesizing information. Excellent knowledge of English language Attention to detail
About us: DivIHN , the 'IT Asset Performance Services' organization, provides Professional Consulting, Custom Projects, and Professional Resource Augmentation services to clients in the Mid-West and beyond. The strategic characteristics of the organization are Standardization, Specialization, and Collaboration.
DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status.