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    Senior Medical Writer

    Synchrony
    3+ years
    Not Disclosed
    Remote
    10 Aug. 22, 2024
    Job Description
    Job Type: Full Time Remote Education: PhD, PharmD, or MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Company Overview

    Join Synchrony Group, a leading network of companies headquartered in West Chester, PA, dedicated to excellence in medical communications. Our mission is to deliver the highest quality products and services, creating value for our clients and opportunities for our team members. We are committed to improving patient outcomes through strategic planning, development, and execution of innovative programs that address medical needs and achieve significant scientific and clinical advancements. Our teams are comprised of medical-scientific, clinical, creative, commercial, and industry experts who work together in an environment of respect and mutual support to make a meaningful impact.

    Position: Senior Medical Writer

    Location: West Chester, PA (Remote work options available)

    Role Overview:

    The Senior Medical Writer will craft original content for a range of publication activities and materials for healthcare professional (HCP) and internal client audiences. This role requires a deep understanding of relevant therapeutic areas and products, the ability to analyze and interpret clinical data, and adherence to industry best practices and guidelines.

    Key Responsibilities:

    • Content Creation: Write original content for publication activities, including primary and review manuscripts, abstracts, posters, slide presentations, and meeting summaries for HCP and internal audiences.
    • Guidelines Adherence: Prepare materials according to internal and client-specific style guidelines, compliance best practices, and journal style guidelines.
    • Data Interpretation: Analyze and apply clinical data to produce high-quality scientific communications.
    • Process Management: Follow internal processes and procedures for workflow, deliverable development, and adherence to industry best practices, including GPP3.
    • Team Collaboration: Work effectively with team members to manage workload, develop and adhere to project timelines, and provide input in team meetings.
    • Client Interaction: Participate in author/client teleconferences, address content-related questions, and lead author teleconferences when necessary.
    • Review and Revision: Efficiently incorporate author/client feedback and review work from medical and freelance writers.
    • Strategic Input: Contribute to brainstorming sessions, strategic publications planning meetings, and new business presentations by synthesizing pharmacologic attributes, clinical data, and market research.

    Internal and External Relationships:

    • Collaboration: Foster relationships with internal and external stakeholders to deliver quality work and innovative solutions.
    • Professionalism: Exhibit a positive attitude and enhance team culture through constructive working relationships and effective communication.
    • Representation: Represent the organization professionally, keeping management informed of key concerns and issues.

    Key Competencies:

    • Attention to Detail: Exceptional scientific and medical accuracy with a keen eye for detail.
    • Problem-Solving: Ability to identify and overcome challenges creatively and strategically.
    • Integrity: High level of ethics, confidentiality, and accountability.
    • Communication: Strong written and interpersonal communication skills.
    • Adaptability: Flexibility to work effectively under time constraints and in a fast-paced environment.
    • Proficiency: Expertise in multiple therapeutic areas and proficiency in Microsoft Office (Word, Excel, Outlook).

    Qualifications:

    • Education: PhD, PharmD, or MD.
    • Experience: Minimum of 3 years in medical communications with substantial professional medical writing experience in various formats.
    • Independence: Ability to work independently on assigned projects.

    Working Conditions:

    • Travel: Willingness to travel as required for client meetings, congresses, and sales meetings.
    • Presentations: Ability to attend and conduct virtual or in-person presentations.
    • Hours: Flexibility to commit to extra or nontraditional hours as needed.

    Additional Information:

    Synchrony Group values the well-being of its employees, offering a comprehensive benefits package that includes competitive salaries, generous paid time off, excellent health insurance, family leave, and a 401(k) plan with employer matching.

    Equal Opportunity Employer:

    Synchrony is committed to a diverse and inclusive workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by federal, state, or local laws.

    Please note that Synchrony is unable to provide visa sponsorship for this role.

    All information will be kept confidential according to EEO guidelines.

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