Publisher II (CSR , IB , Protocol publishing)

Description

Publisher II (CSR , IB , Protocol publishing)

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 brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

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 and engaged 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. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. Why Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.

Job Responsibilities

Primary responsibility for all components of document compilation and publishing
. Requires good working knowledge of FDA, EU, ICH and ISO guidelines to ensure submission
documents meet or exceed sponsor and regulatory requirements and guidance.
. Responsible for the thorough peer review of published documents created within or outside of
the Company, when applicable.
. Interacts with medical writers and medical editors in the medical writing department
. Interacts with cross-functional project teams within the Company (Project Leads, Clinical, Data
Management, Regulatory Consulting, and Biostatistics), and with clients as applicable.
. Assists in training and mentoring Publisher I staff.
. Performs other work-related duties as assigned.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, 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.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Summary

Provides advanced document-level compilation and publishing services for Medical Writing, including clinical study reports (CSRs) protocols and protocol amendments investigator brochures annual reports, and other regulatory documents that meet current ICH electronic document requirements and guidelines. Interacts with the medical writing department and with project teams within the company (Project Leads, Clinical, Data Management, Regulatory Consulting, Biostatistics), and in some cases direct contact with clients to ensure that all regulatory specified documents are complete, accurate, and compatible with sponsor and regulatory agency software programs.