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:
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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.)
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Conducts literature scans/searches and review for summaries and reports
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Proactively incorporates team input and comments into edits and revisions.
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Performs and completes quality review and verification vs source data.
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Completes project/workstream/ClinChoice specific work instructions (WI), process guidelines, SOP trainings as per identified schedule.
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Contributes knowledge on diverse topics within the Medical Device arena.
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Streamlines the clinical research writing approach to ensure that clinical and epidemiologic data are presented coherently
Requirements:
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Allied health professional, such as a Medical Doctor, Nurse, or Pharmacist
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Well versed in medical terminology, anatomy, and
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Experience in copy review/copy
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Project management
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With experience in supporting the medical device or pharma
Our Benefits:
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Daily Meal Subsidy
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Flexible working hours and work from home privileges.
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HMO coverage up to maximum of 2 dependents subsidy
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Life and accident Insurance
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15 Sick Leave and 15 Vacation Leave
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Monetized leave
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Performance Based Annual Salary Increase
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Clothing Allowance
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Rice Allowance
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Laundry Allowance