clinchoice

ClinChoice is seeking a Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence in the Philippines. The role provides safety oversight for the Consumer portfolio across the product life cycle and partners with RMSO on regional safety deliverables.The incumbent collaborates with LPV country teams and cross-functional...

ClinChoice in Manila is seeking a senior clinical programmer to support FDA submissions. The role focuses on SDTM/ADaM data generation using SAS, creating tables, listings, and graphs for CSR, posters, and manuscripts. You will aid in ISS/ISE deliverables and define.xml packaging under GMP guidance.Requires 4+ years of clinical programming with strong...

ClinChoice Philippines is seeking a Medical Physician with at least 2 years of experience as a Medical Reviewer for IC SRS to join our pharmacovigilance team. You will conduct medical reviews focusing on seriousness, causality, and narrative quality, ensuring compliance with ICH-GCP, GVP modules, and applicable regulatory guidelines.You will work across...

ClinChoice in Pasig, Philippines, is seeking a Scientist/Senior Scientist for the QPPV Office, Local Safety Support & Regulatory Intelligence. This role focuses on safety oversight for the Consumer portfolio throughout product lifecycles, including development, with strong emphasis on collaboration with RMSO and regional teams.The candidate will provide...

ClinChoice in the Philippines seeks an experienced Clinical Programmer to annotate CRFs, develop SDTM/ADaM datasets, and generate Tables, Listings and Graphs for CSR and manuscripts. You will contribute to eSubmission packages to FDA and collaborate with global statisticians. The role requires 4+ years in clinical programming, strong SAS skills, and...

JOB DESCRIPTION Summary: The ERP System Operations Project Manager leads the international arm of ClinChoice’s Global ERP Administration function and collaborates with the company’s international cross-functional teams to support users in their day-to-day use of Microsoft Dynamics 365. The role also works with the company’s ERP development team and...

Job Description: Help guide report strategy, help determine important safety concerns and review medical and medical safety content that will be included or discussed in the report, including but not limited to safety signals, health authority requests, safety-related literature, adverse event case reviews, benefit-risk assessments, and overall medical...

Responsibilities: Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines. Develop SDTM specifications and generate SDTM datasets using SAS. Develop ADaM specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan. Develop Tables, Listings, Graphs, Patient Profile in support of the Clinical Study Report,...

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,...

Job Description:  The Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence is a safety expert who provides safety oversight, in their allocated region, for the Consumer portfolio of products throughout the life cycle of the products, including new product development. The incumbent works closely with and partners with...

Job Description: Responsibilities: Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines. Develop SDTM specifications and generate SDTM datasets using SAS. Develop ADaM specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan. Develop Tables, Listings, Graphs, Patient Profile in support of the...

Primary Responsibilities:Awareness and understanding of relevant GVP modules.Perform medical review of non-serious & serious IC SRS with emphasis on seriousness, expectedness, causality & narrative etc. without missing on quality & compliance.Experience of medical review of IC SRS received from sources such as Spontaneous, Literature, Regulatory Authority,...

Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory IntelligencePasig, PhilippinesJob Description:The Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence is a safety expert who provides safety oversight, in their allocated region, for the Consumer portfolio of products throughout the life cycle...

Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence Pasig, Philippines Job Description: The Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence is a safety expert who provides safety oversight, in their allocated region, for the Consumer portfolio of products throughout the life...

Responsibilities: Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines. Develop SDTM specifications and generate SDTM datasets using SAS; Develop ADaM,specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan; Develop Tables, Listings, Graphs, Patient Profile in support of the Clinical Study Report,...

Job Responsibilities: Perform general administrative tasks in support of the HR team. Assist with recruitment, maintaining files, and data entry. Support onboarding and HR communications. Prepare HR documentation and forms. Maintain HR records and filing systems. Assist with HR reporting and analytics. Support training and orientation logistics. Assist with...

JOB DESCRIPTION: Educational Qualification: Bachelor of Science in Accountancy student Responsibilities: To assist in checking and completing 2025 and 2026 files. Filing and printing of documents Other specifications: Honest and responsible Computer Literate Can work with minimum supervision, self-starter

About ClinchoiceClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with...

About ClinchoiceClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with...

Responsibilities: The Project Coordinator, Shared Services acts as the project management process owner. This role focuses on process optimization and the deployment and utilization of consistent project management methodologies in support of the execution of Periodic Safety Update Reports.   Knowledge and access to applicable Medical Device Quality...