Medical Writer, Scientific Communications
Job Description:
• Prepare high-quality abstracts and presentations for submission and presentation at conferences.
• Engage in scientific writing and/or edit manuscripts for submission to peer-reviewed journals to achieve publication goals.
• Ensure scientific communication deliverables are completed in a timely manner.
• Evaluate data and translate information into succinct, scientific summaries.
• Collaborate cross-functionally with clinical, marketing, and creative teams to ensure data dissemination goals and deadlines are met.
• Work with clinical study management and statistics teams to create timelines for completing data dissemination plans related to clinical studies.
• Strong communication with physician authors to achieve deliverables, maintain relationships, and to facilitate overall scientific communication efforts.
• Contribute to the preparation of clinical data for analysis and scientific writing.
• Conduct literature searches for relevant disease states and maintain the clinical literature library.
• Lead cross-functional project reviews and serve as a core team member and subject matter expert on clinical study teams to create timelines for completing medical writing documents.
• Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. *
• Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company. *
• Ensure other members of the department follow the QMS, regulations, standards, and procedures. *
• Perform other work-related duties as assigned.*Indicates an essential function of the role
Requirements:
• Advanced degree (Master’s, PhD, or MD) with 2+ years of experience as a medical writer in the medical device, biotech, or pharmaceutical industry; or 5+ years of experience as a medical writer in clinical/scientific research, or an equivalent combination of education and experience.
• Experience as a medical writer for cardiovascular clinical trials in the medical device, biotech, or pharmaceutical industries is preferred.
• Demonstrates a diligent approach to work, with a portfolio that showcases outstanding writing skills and a passion for clarity in written expression.
• Team player with excellent organizational skills and the ability to prioritize assignments and manage multiple projects simultaneously, both independently and collaboratively.
• Proficient in Microsoft Office 365.
• Familiarity with laws, regulations, standards, and guidance governing the conduct of clinical studies a plus.
Benefits:
• A collaborative teamwork environment where learning is constant, and performance is rewarded.
• The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
• A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).
Apply tot his job
Apply To this Job
• Prepare high-quality abstracts and presentations for submission and presentation at conferences.
• Engage in scientific writing and/or edit manuscripts for submission to peer-reviewed journals to achieve publication goals.
• Ensure scientific communication deliverables are completed in a timely manner.
• Evaluate data and translate information into succinct, scientific summaries.
• Collaborate cross-functionally with clinical, marketing, and creative teams to ensure data dissemination goals and deadlines are met.
• Work with clinical study management and statistics teams to create timelines for completing data dissemination plans related to clinical studies.
• Strong communication with physician authors to achieve deliverables, maintain relationships, and to facilitate overall scientific communication efforts.
• Contribute to the preparation of clinical data for analysis and scientific writing.
• Conduct literature searches for relevant disease states and maintain the clinical literature library.
• Lead cross-functional project reviews and serve as a core team member and subject matter expert on clinical study teams to create timelines for completing medical writing documents.
• Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. *
• Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company. *
• Ensure other members of the department follow the QMS, regulations, standards, and procedures. *
• Perform other work-related duties as assigned.*Indicates an essential function of the role
Requirements:
• Advanced degree (Master’s, PhD, or MD) with 2+ years of experience as a medical writer in the medical device, biotech, or pharmaceutical industry; or 5+ years of experience as a medical writer in clinical/scientific research, or an equivalent combination of education and experience.
• Experience as a medical writer for cardiovascular clinical trials in the medical device, biotech, or pharmaceutical industries is preferred.
• Demonstrates a diligent approach to work, with a portfolio that showcases outstanding writing skills and a passion for clarity in written expression.
• Team player with excellent organizational skills and the ability to prioritize assignments and manage multiple projects simultaneously, both independently and collaboratively.
• Proficient in Microsoft Office 365.
• Familiarity with laws, regulations, standards, and guidance governing the conduct of clinical studies a plus.
Benefits:
• A collaborative teamwork environment where learning is constant, and performance is rewarded.
• The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
• A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).
Apply tot his job
Apply To this Job