Senior Medical Content Strategist
hace 6 días
About Syneos Health
Syneos Health is a leading biopharmaceutical solutions organization, built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes that address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything we do. We are continuously looking for ways to simplify and streamline our work, making Syneos Health easier to work with and for.
We are agile and driven to accelerate the delivery of therapies because we are passionate about changing lives.
- Work Here Matters Everywhere
- Why Syneos Health
We are passionate about developing our people through career development and progression, supportive and engaged line management, technical and therapeutic area training, peer recognition, and total rewards programs.
We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
Job Responsibilities:- Maintains familiarity with FDA, EU, and other relevant guidelines and industry standards to ensure that documents meet or exceed sponsor and regulatory requirements and guidance.
- Represents the editorial group in Medical Writing, on study teams, and in cross-departmental project teams as needed.
- Monitors timelines and budgets for assigned projects and updates the Lead Medical Writer, Project Manager, and/or direct supervisor (as appropriate) if deliverables are at risk.
- Provides technical support and expertise as appropriate.
- Conducts training of medical editing staff and functions as a mentor.
- Advises medical writers, medical editors, and study teams on data integrity review, compilation, publishing, and editorial standards.
- Provides training to members of the global Medical Writing team in aspects relative to their roles.
- Project lead for deliverables of assigned complex and/or large medical writing projects, including but not limited to scheduling and leading internal project-specific team meetings, organizing project-specific requirements, and ensuring that all information is distributed to the editorial team and implemented within the deliverable.
- Serves as a member of the medical writing team for projects with medical writing deliverables.
- Provides feedback to the lead medical writer on progress of document editorial process.
- Copyedits assigned documents, applying correct grammar, punctuation, spelling, and style following American Medical Association (AMA) or various custom style guidelines as well as established medical writing internal checklists and best practices.
- Performs data integrity review of assigned documents to ensure accuracy.
- Contributes to the development of process improvement tools and the development or revision of internal policies and procedures affecting editorial work.
- Manages assigned projects according to medical writing standard operating procedures and client standards, on time and on budget.
- May compile and publish medical writing deliverables.
$80,000 - $100,000 per year
Qualifications:- Bachelor’s degree (preferred) in the life sciences, clinical sciences, or English/journalism; or copyediting, data integrity review, and/or relevant publishing experience.
- Significant relevant publishing experience using Adobe Acrobat or other appropriate markup language preferred; ISIToolbox experience preferred.
- Strong proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint).
- Excellent attention to detail, including strong copyediting, data integrity review, accuracy, problem-solving, organizational, interpersonal, presentation, project management, and team-oriented skills.
- Excellent grammatical and communication skills, both written and oral.
- Extensive familiarity with the AMA style guide strongly preferred.
- Ability to work with minimal supervision on multiple assignments with set deadlines.
- Ability to work independently as well as part of a team and keep others informed of the progress and status of projects.
- Adaptable to changes in work duties, responsibilities, and requirements.
- Knowledge of FDA and EU requirements, ICH regulations, and ISO standards as applicable to regulatory documents preferred.
Syneos Health has worked with 94% of all Novel FDA Approved Drugs over the past 5 years. No matter your role, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.
Learn more about Syneos Health
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