Sr. Scientist, Medical Review Physician job opportunity at ClinChoice.



bot
ClinChoice Sr. Scientist, Medical Review Physician
Experience: 5-years
Pattern: full-time
apply Apply Now
Salary:
Status:

Safety

Copy Link Report
degreeAssociate
loacation Pasig City,, Philippines
loacation Pasig City,....Philippines

Primary Responsibilities: Awareness and understanding of relevant GVP modules. Perform medical review of non-serious & serious ICSRs with emphasis on seriousness, expectedness, causality & narrative etc. without missing on quality & compliance. Experience of medical review of ICSRs received from sources such as Spontaneous, Literature, Regulatory Authority, Solicited and Clinical trials. Experience across multiple therapeutic areas such as Oncology, Respiratory, Immunology, Neuroscience, Rare diseases etc. Support triage of cases and determine seriousness and relatedness across products as assigned. Review and verify appropriate selection of adverse events from source documents, assign appropriate MedDRA code, assess labelling and review narrative. Acquire and maintain current knowledge of product portfolio and safety profiles for products across therapeutic areas.  Involve in process improvement activities such as implementation of quality control process. Provide medical guidance and expert opinion on the cases to the data entry associates and quality reviewers to help resolve queries. Identify and resolve case issues, coordinate with client therapeutic teams and within functional team and manage as appropriate. Maintain PV expertise, and understanding of international safety regulations and guidelines.  Responsible for completing the MR activities in the safety database within the stipulated time to comply with service level agreements and regulatory timelines. Provide timely feedback to case processors on the errors/ discrepancies noted.  Assist in training/mentoring of other case processing/medical review personnel as necessitated. Adapt to different client case processing conventions and multi-task as per business needs. Perform ad-hoc tasks as advised by the team lead/manager with quality and compliance as per project requirement. Participate in organizational activities to meet objectives suitable for the role/area of expertise. Candidate Profile: Should be a MBBS/MD with 4 - 5 years of experience as Medical Reviewer for ICSRs.  Must possess thorough knowledge of ICH-GCP, relevant GVP module, 21 CFR guidelines and other regulatory requirements. Training and mentoring skill (GVP concepts & medical aspects such as disease condition, product portfolio etc) Must have hands on experience with MS Office applications (Outlook, Excel, Word, Power Point etc.).

Other Ai Matches

Associate, Project Management (PSUR) Applicants are expected to have a solid experience in handling Medical Affairs related tasks
Manager, Accounting Applicants are expected to have a solid experience in handling Finance related tasks
Drug Safety Associate Consultant Applicants are expected to have a solid experience in handling Safety related tasks
Senior Statistical Programmer / Analyst III Applicants are expected to have a solid experience in handling Statistical Programming related tasks
Regulatory Affairs Specialist – Consultant Applicants are expected to have a solid experience in handling Regulatory Affairs related tasks
Quality Assurance Manager Applicants are expected to have a solid experience in handling External Quality Assurance related tasks
Quality Assurance Specialist Applicants are expected to have a solid experience in handling External Quality Assurance related tasks
Associate, Regulatory Affairs Applicants are expected to have a solid experience in handling Regulatory Affairs related tasks
Associate, Legal Affairs Applicants are expected to have a solid experience in handling Legal Affairs related tasks
Senior/Principal Statistical Programmer Analyst/Consultant-Oncology Applicants are expected to have a solid experience in handling Statistical Programming related tasks
Medical Reviewer Consultant Applicants are expected to have a solid experience in handling Medical Writing related tasks
Data Scientist with R programming skills and clinical trial exposure Applicants are expected to have a solid experience in handling Statistical Programming related tasks
Regulatory Affairs Associate - CONSULTANT Applicants are expected to have a solid experience in handling Regulatory Affairs related tasks
Clinical R Programmer (SDTM/ADaM) Contract role- remote Applicants are expected to have a solid experience in handling Statistical Programming related tasks
1478# Associate Director, Statistical Programming Permanent Role - Hybrid Applicants are expected to have a solid experience in handling Statistical Programming related tasks
Associate - Regulatory Affairs (RMQ) Applicants are expected to have a solid experience in handling Regulatory Affairs related tasks
Clinical Research Associate II and Senior Clinical Research Associate Applicants are expected to have a solid experience in handling Strategic Resourcing related tasks
Clinical Research Associate II and Senior Clinical Research Associate Applicants are expected to have a solid experience in handling Strategic Resourcing related tasks
Associate, Accounting Applicants are expected to have a solid experience in handling Finance related tasks
Director Statistical Programming- Permanent role at UK Applicants are expected to have a solid experience in handling Statistical Programming related tasks
Senior Associate - CMC5 Applicants are expected to have a solid experience in handling Regulatory Affairs related tasks
Sr. Scientist, Medical Review Physician Applicants are expected to have a solid experience in handling Safety related tasks
Senior Regulatory Consultant- Lead Applicants are expected to have a solid experience in handling Regulatory Affairs related tasks