Scientist, Medical Writing at ClinChoice

Pasig, Metro Manila, Philippines -

Full Time

Start Date

Immediate

Expiry Date

08 Jun, 26

Salary

0.0

Posted On

10 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Study Documents Review, Clinical Study Reports (CSR), Study Protocols/Synopses, Informed Consent (IC), Investigator’s Brochure (IB), Safety Management Plan, Safety Reports (PBRERs), DSURs, PADERS, Literature Scans/Searches, Quality Review, Verification vs Source Data, Work Instructions (WI), Process Guidelines, SOP Trainings, Medical Device Arena Knowledge

Industry

Pharmaceutical Manufacturing

Description

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 Requirements: 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 Our Benefits: • 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

Responsibilities

The role involves assisting in the development and review of various clinical study documents such as CSRs, protocols, and safety reports, while also conducting literature reviews and ensuring quality verification against source data. Responsibilities include adhering to internal work instructions and contributing specialized knowledge within the Medical Device sector.