• Lead the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity • Collaborate closely with cross-functional teams, including clinical research, biostatistics, regulatory affairs, and medical affairs, to interpret and analyze clinical trial data, summarize scientific findings • Participate in the planning and execution of clinical development programs, providing strategic input and scientific expertise to support the design, conduct, and interpretation of clinical studies and research initiatives. • Contribute to the development of publication plans, abstracts, posters, and manuscripts for submission to peer-reviewed journals and presentation at scientific conferences • Mentor and coach junior medical writers, providing guidance on best practices, writing techniques, and scientific principles, and fostering a culture of excellence, collaboration, and continuous learning within the medical writing team.

Role Description As a SSBV Clinical Claims Review RN, you can put your skills and talents to work in a multifaceted role that is highly rewarding. You will be accountable for making decisions that directly impact our members while managing a demanding case load in a rapidly changing, production-driven environment. You will enjoy the flexibility to telecommute* from anywhere within the U.S. as you take on some tough challenges. Primary Responsibilities: - Perform administrative reviews of short stay inpatient hospital claims in accordance with Federal, State and client specific requirements - Responsible for documentation of all determinations - Maintain accurate use of screening criteria Qualifications - Associate's degree - Current and unrestricted RN license in the state of residency - 5+ years of clinical documentation experience - 3+ years of experience as an RN, including inpatient/acute setting - Intermediate level of proficiency in Microsoft Office (to include Microsoft Excel and One Note) - Intermediate level of proficiency in writing - Designated home office workspace with access to install secure high-speed internet via cable/DSL Requirements - Undergraduate or higher degree (preferred) - A background in utilization review for an insurance company or experience in case management (preferred) - Familiarity with InterQual and/or MCG Care Guidelines (preferred) - Critical thinking skills (preferred) Benefits - Paid Time Off which you start to accrue with your first pay period plus 8 Paid Holidays - Medical Plan options along with participation in a Health Spending Account or a Health Saving account - Dental, Vision, Life & AD&D Insurance along with Short-term disability and Long-Term Disability coverage - 401(k) Savings Plan, Employee Stock Purchase Plan - Education Reimbursement - Employee Discounts - Employee Assistance Program - Employee Referral Bonus Program - Voluntary Benefits (pet insurance, legal insurance, LTC Insurance, etc.)

Title: Medical Writer - Medical Information Location: Remote North Carolina United States of America Full time Remote   The Medical Writer will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.   Job Responsibilities: - Develops and updates standard medical response documents, custom response documents, frequently asked questions, and Academy of Managed Care Pharmacy formulary dossiers, specific to the peri- and post-approval phases of the product lifecycle. - Researches and responds to escalated medical information inquiries from healthcare providers. - Conducts literature searches for standard response documents utilizing secondary databases.  - Utilizing professional judgment, integrates  pertinent clinical data into standard response documents with clear, concise, accurate and balanced medical writing following organizational, client, and regulatory guidelines. - Participates as required in project launch meetings, review meetings, and project team meetings, serving as a liaison for communication with the client. - Collaborates and effectively communicates with internal and external client contacts to provide high quality medical information writing deliverables in a timely manner and within budget.   Education and Experience: - PharmD - Experience with Medical Information (equivalent to 2+ years) - Previous experience that provides the knowledge, skills and abilities to perform the job (comparable to 2+ years) - Experience working in the pharmaceutical/CRO industry preferred   Knowledge, Skills, and Abilities: - Solid medical writing skills, including grammatical, editorial and proofreading skills - Ability to interpret and present complex data accurately and concisely - Effective administrative, organizational and planning skills; attention to detail and quality - Ability to work on own initiative and effectively within a team - Effective oral and written communication skills - Great judgment and decision-making skills - Good computer skills and skilled with client templates; good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)

• Collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence. • May serve as a primary writer who creates and provides input on routine deliverables, such as medical information documents. • Ensures compliance with applicable SOPs, WI, quality processes, and requirements for documents. • May assist in determining best practices for achieving optimal results. • May assist in program management activities. Duties could include developing timelines and budgets for assigned deliverables and tracking deliverable metrics.