ichs jobs in Pasig

Syneos Health Philippines, Inc. is seeking a (Sr.) Project Associate to drive planning and execution of clinical trial elements in collaboration with the Project Lead.You will oversee timelines, budgets, and resource coordination, while mentoring junior staff in a global life sciences environment. The role requires strong organizational and communication...

This is a fully remote position, open to candidates based in Philippines. Pay: $30–$60/hr Role Title: Medical Writer (Pharmaceutical) Role Type: Contractor Location: Remote We are engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical...

Thermo Fisher Scientific is seeking a PV Coordinator in the Philippines to provide contracted project coordination and safety support on global and domestic programs. You will review adverse events, support Data Safety Monitoring Boards and Endpoint Adjudication Committees, and liaise with Safety Specialists and Medical Monitors to ensure timely reports and...

RemoteJobsOne is seeking a Medical Writer (Pharmaceutical) for a fully remote contractor role based in the Philippines. You will help train AI-assisted clinical documentation tools by applying regulatory writing expertise to ensure high-quality inputs and model learning. The ideal candidate has 5+ years of regulatory medical writing, deep knowledge of ICH E3...

Cromos Pharma, an international contract research organization, seeks a capable professional to support CRAs in routine activities and help coordinate regulatory document submission. The role involves safety data reporting, remote monitoring, and site management across European projects.Candidates should hold a science-related degree or be pursuing one, with...

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 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...

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...

This is a fully remote position , open to candidates based in Philippines. Pay: $60–$65/hr Role Title: Biostatistician Role Type: Contractor Location: Remote We are engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Regulatory PharmacistRivermed, IncSalary: ₱25-30K [Monthly] On-site - PasigExperience: 1-3 Yrs ExpBachelor Full-timeJob DescriptionPrepare, review, and submit product registration dossiers to the FDA (Food and Drug Administration) and other relevant regulatory bodies.Ensure all products comply with local laws and regulations, including labeling,...

The Clinical Data Manager, will participate in various clinical data management activities required to ensure that data captured in a few clinical trials undertaken, or managed by Innovaderm, are collected, managed and reported clearly, accurately and securely. In addition, this position is required to conduct all these activities in conformance with...

The Clinical Study Builder will work closely with data management and statistical staff to design and develop electronic case report forms (eCRFs), visit schedules and associated data quality checks for medical research studies. This position is required to work in a dynamic and collaborative environment. In addition, solution creation includes...

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...

About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best‑in‑class and first‑in‑disease therapeutic candidates that directly target...

(Sr.) Project Associate, Philippines Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions...

Job OverviewProvide comprehensive clinical lab data expertise as part of a team to develop and maintain Laboratory Data Management (LDM) tasks for the studies awarded to IQVIA Laboratories and meets the external client data reporting needs. May be required to support the development of new systems and processes related to the electronic data transfer...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a PV Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Associate Safety Admin - Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our...

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,...