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Epidemiology Medical Writer Manager, RWE ** open to several EMEA and LATAM countries (Remote) **
Updated: Today
Location: AZ, United Arab Emirates
Job ID: 25107871-OTHLOC-4585-2DR
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Description
Epidemiology Medical Writer Manager, RWE ** open to several EMEA and LATAM countries (Remote) **Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
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 deliver – for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
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 building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
JOB SUMMARY
The Research Manager, Real World Evidence (RWE) is responsible for executing a variety of claims database analyses, prospective and retrospective multi-site observational studies, and patient reported outcomes studies, producing high quality RWE research and raising awareness of RWE.
JOB RESPONSIBILITIES
A significant portion of this role is dedicated to medical writing, supporting the design and execution of Real World Evidence (RWE) studies. The individual will contribute to the development of study protocols across a range of methodologies, including global and regional healthcare claims database studies, multi-site observational studies, Patient-Reported Outcomes (PRO) studies, and systematic literature reviews. This role requires close collaboration with cross-functional teams to ensure scientific rigor, clarity of research objectives, and high-quality, client-ready deliverables.
- Responsible for delivery of project outputs that are within budget and timelines and meet quality standards.
- With oversight, prepare draft study reports and external publications.
- Contribute to the development of materials for congress presentations and manuscripts.
- Primary sponsor contact for assigned projects.
- Participate in business development activities.
QUALIFICATION REQUIREMENTS (please indicate if ‘preferred’)
- Advanced degree (Master’s) in epidemiology, economics, public health or other health related fields or acceptable equivalent combination of education and experience.
- At least two years’ experience writing protocols, study reports, and similar documents for RWE/RWLP work
- The ability to develop understanding of retrospective and prospective research methods, phase IIIB/IV study designs, HEOR and related methodology.
- Strong personal communication and good teamwork skills
- Candidate must demonstrate regional Real World Research experience.
- Other experience includes extensive experience with personal computers; knowledge of statistical software.
- Fluent in written English. Regional language fluency is preferred (Japanese, Chinese, Korean).
- Excellent communication, presentation, interpersonal skills, both written and spoken.
- Ability to travel as necessary (approximately 10-15%).
Disclaimer:
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.
FLSA status: Exempt
Years of experience required: Minimum of three (3) to five (5) years related industry experience.
Physical Requirements: Position requires: ability to occasionally move about inside the office to access filing cabinets, office equipment, etc. and to move between office locations; ability to maintain a stationary position for prolonged periods of time; ability to occasionally manipulate (e.g., lift, carry, move) office items and packages of light to medium weights of 10-35 pounds; ability to constantly operate a computer and other office productivity equipment (e.g., scanner, phone, printer, copier); ability to perceive and assess written materials for prolonged periods of time; and ability to frequently communicate with colleagues on the phone, by email, and in-person.
Work Environment: This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets. The noise level in the work environment is low. This is a largely sedentary role.
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
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