Scientist Medical Writing

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Clinical Scientist on a permanent basis, while working on projects from our varied client base, ranging from small to big pharmaceutical, biotechnology, medical device, and consumer health companies.

Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!

Main Job Tasks and Responsibilities:

• Assists in developing and review of clinical study documents: clinical study reports (CSR), study protocols/synopses, informed consent (IC), investigator’s brochure (IB), safety management plan, and safety reports (PBRERs, DSURs, PADERS, etc.)
• Conducts literature scans/searches and review for summaries and reports
• Proactively incorporates team input and comments into edits and revisions.
• Performs and completes quality review and verification vs source data.
• Completes project/workstream/ClinChoice specific work instructions (WI), process guidelines, SOP trainings as per identified schedule.
• Contributes knowledge on diverse topics within the Medical Device arena.
• Streamlines the clinical research writing approach to ensure that clinical and epidemiologic data are presented coherently
  
  
  

• Allied health professional, such as a Medical Doctor, Nurse, or Pharmacist
• Well versed in medical terminology, anatomy, and
• Experience in copy review/copy
• Project management
• With experience in supporting the medical device or pharma
  
  
  

• Daily Meal Subsidy
• Flexible working hours and work from home privileges.
• HMO coverage up to maximum of 2 dependents subsidy
• Life and accident Insurance
• 15 Sick Leave and 15 Vacation Leave
• Monetized leave
• Performance Based Annual Salary Increase
• Clothing Allowance
• Rice Allowance
• Laundry Allowance