ichs jobs in Manila

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...

SciGen Pte. Ltd. is seeking a Regulatory Affairs Specialist to support registration, maintenance, and compliance of pharmaceutical products. The role spans regulatory affairs, quality assurance, and pharmacovigilance, ensuring adherence to FDA requirements and company procedures. Responsibilities include dossier reviews, submissions, labeling checks,...

Fortrea is pooling candidates in Manila for future CRA and clinical operations opportunities. The role focuses on site management for oncology studies, ensuring regulatory and data integrity obligations are met across audits and visits.Ideal candidates have at least 2 years of site monitoring experience in oncology, with exposure to start-up, maintenance,...

Fortrea Philippines is seeking a Safety Data Management professional to respond to medical information requests and process adverse drug reaction cases. The role involves call intake, data entry, and ensuring regulatory timelines and data quality.The candidate should have a pharmacy or life sciences background with 1–2 years in safety, and familiarity with...

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...

Note: This job post is for POOLING candidates for future CRA and/or clinical operations opportunities.Summary of ResponsibilitiesSite management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records....

OrciMed Life Sciences Philippines OPC in Manila is seeking a Clinical Trial Manager to lead day-to-day clinical operations across CROs, sites, and vendors, ensuring on-time, compliant delivery of monitoring and study activities. You will collaborate with cross-functional teams to align expectations and manage risk while maintaining study integrity.The role...

Summary of Responsibilities: To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Receive information, record, and report Adverse Drug Reaction in timelines (according to the regulations and to internal WI/SOPs) that may be received over telephone calls, email, fax...

Summary of Responsibilities To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Receive information, record, and report Adverse Drug Reaction in timelines (according to the regulations and to internal WI/SOPs) that may be received over telephone calls, email,...

Fortrea Philippines Inc. in Manila is seeking a Pharmacovigilance Specialist to respond to medical information queries, receive and document adverse events, and ensure timely reporting and data accuracy.You will handle inquiries via phone, email, and other channels with a focus on quality and compliance. The role requires strong communication, familiarity...

About the roleThe Clinical Trial Manager (CTM) will work collaboratively across cross-functional teams with Project Management, Clinical Operations, Data Management, Medical Monitoring, Pharmacovigilance, and Regulatory Affairs while understanding and managing client expectations. The Clinical Trial Manager is responsible for the day-to-day management of...

Summary of ResponsibilitiesTo respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc.Receive information, record, and report Adverse Drug Reaction in timelines (according to the regulations and to internal WI/SOPs) that may be received over telephone calls, email, fax...

## Clinical Data Coordinator (Philippines)Remote - English - Philippines · Permanent · Entry-level#### About The PositionThe Clinical Data Coordinator will participate in various clinical data management activities required to ensure that data captured in clinical trials undertaken, or managed by Indero, are collected, managed and reported clearly,...

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...

CRA - PHL At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients...

(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...

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...

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

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

The Regulatory Affairs Specialist is responsible for supporting regulatory activities related to the registration, maintenance, and compliance of pharmaceutical products as well as Quality Assurance and Pharmacovigilance activities to ensure adherence to FDA requirements, applicable regulations, and company procedures. Key Responsibilities: Regulatory...