Medical Editor II - (Formatting Regulatory Documents) - Home Based

Syneos Health, Inc.; A distancia; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading biopharmaceutical solutions organization is seeking a Medical Editor II to ensure quality formatting of clinical and regulatory documents. The role involves defining formatting scopes, coordinating activities, and conducting quality reviews. Ideal candidates will possess strong attention to detail and communication skills. This home-based position emphasizes inclusion and career development, contributing to a dynamic team focused on customer success.

Servicios

Career development and progression

Engaged line management

Total rewards program

Formación

• Responsible for formatting clinical and regulatory documents to comply with guidelines.
• Experience with formatting standards and styles in a medical or regulatory context is required.

Responsabilidades

• Defines the scope of formatting for clinical and regulatory documents.
• Coordinates and tracks activities, performing detailed quality reviews.
• Ensures document format and styles are consistent with defined templates.
• Maintains strong knowledge of regulatory information management systems.

Conocimientos

Attention to detail

Interpersonal communication skills

Organizational skills

Conflict management

Descripción del empleo

Medical Editor II - (Formatting Regulatory Documents) - Home Based

Updated: December 3, 2025
Location: Madrid, Spain
Job ID:25102337-OTHLOC-3529-2DMAD-2DR

Description

Medical Editor II - (Formatting Regulatory Documents) - Home Based

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.

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

Roles and Responsibilities:

• Defines scope of formatting of clinical and regulatory documents with the document author. Coordinates and track activities and perform detailed quality reviews. Import and route documents in the regulatory information management systems (RIMS).
• Ensure document format and styles are consistent with the defined in RIMS and are consistent with the clinical and regulatory templates. Ensure document properties and naming conventions are used. Maintain strong knowledge of RIMS styes and formatting standards.
• Effectively communicates deliverables needed to stakeholders. Must demonstrate good interpersonal and organizational communication skills, including conflict management skills.
• Effectively attends to multiple tasks within overlapping timeframes; builds positive and productive relationships that enable high quality documents to be completed on time.

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

Responsible for ensuring the quality of clinical and regulatory documents are formatted to the requirements in the AbbVie style guide and document templates.