Overview Updated: September 16, 2025 • Location: ESP-Remote (Barcelona) • Job ID: 25101798
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model centers the patient and the customer, and we collaborate across functional service provider or full-service environments to accelerate delivery of therapies.
Discover what our 29,000 employees across 110 countries already know: WORK HERE MATTERS EVERYWHERE
Why Syneos Health We are passionate about developing our people through career development and progression; supportive line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to our Total Self culture – where you can authentically be yourself and be cared for as part of a global team.
We value diversity of thoughts, backgrounds, and perspectives to create a sense of belonging for everyone.
Job Responsibilities Develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring standards, as applicable, in adherence with study/project timelines and corporate objectives.
Manage medical writing projects, including developing timelines (in coordination with study/project teams) and communicating with cross-functional team members to maintain awareness of review cycles and expectations.
Participate in cross-functional meetings to provide input on medical writing deliverables, timelines, and any processes needed for the completion of regulatory documents.
Review other documents associated with the assigned projects (e.g., Protocols and Statistical Analysis Plans), as appropriate.
Participate in cross-functional process improvement initiatives and define/write standard operating procedures and best practices for efficient preparation of quality documents.
Manage internal and contract medical writing resources to ensure timely completion of assigned projects.
Mentor more junior medical writing staff.
Salary and Benefits Salary Range: $114,000.00 - $210,900.00
The base salary range represents the anticipated low and high range for this position. Actual salary will vary based on qualifications and experience. Benefits may include medical, dental, vision, 401(k) matching, stock purchase plan eligibility, incentive bonuses, and flexible PTO; eligibility for paid sick time varies by location. Syneos complies with applicable paid sick time requirements.
Benefits & Additional Information Company car or car allowance (where applicable)
Health benefits (Medical, Dental, Vision)
401(k) with company match; Employee Stock Purchase Plan eligibility
Bonuses/commissions based on company and individual performance
Flexible paid time off and paid sick time as required
Equal Opportunity Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status. Reasonable accommodations are available to applicants with disabilities upon request.
About the Role The Senior Principal Medical Writer leads development of clinical documents for regulatory submissions, provides strategic direction to cross-functional teams, mentors writers, and oversees medical writing activities for multiple compounds. Requires broad understanding of clinical research processes and global regulatory standards.
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