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Medical Writer (Applicant with 4 Years of experience in Document QC)


Location

Gurgaon | India


Job description

Clinical Project Coordinator

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

Description

This role is responsible for tracking the request management systems, maintaining IIS request and External funding database, performing QC checks on IIS request and process them within platform developing other high-quality documents. The candidate need to possess excellent analytical and communication skills (both written and verbal) and good attention to details. They should be well adept with MS Office applications.

Responsibilities

Qualifications

What we’re looking for
•     Masters of Degree in Any Lifescience Domain with 3 –4 years of healthcare and life science domain experience .
•    Experience in Domain like TMF QC, Narrative QC etc will be preferred . 
•    Understanding of FDA and ICH regulations and guidelines strongly preferred. 
•    Demonstrated effective presentation, proofreading, and interpersonal, skills and ensure a team-oriented approach. 
•    Strong proficiency in Word, Excel, PowerPoint, email, and Internet. 
•    Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information. 

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.


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