Clinical Trial Hub Safety Associate Professional

Job OverviewWe are seeking a highly skilled Clinical Trial Hub Safety Associate to join our team at Pfizer.SalaryThe estimated salary for this role is $80,000 - $110,000 per year, depending on location and experience.About the RoleIn this critical position, you will play a vital role in ensuring the safe and appropriate use of medicines for patients through...

About ClarioClario is a leading endpoint technology solutions provider for clinical trials. With over 19,000 clinical trials delivered in support of 870 regulatory approvals, we have gained extensive scientific expertise and global scale. Our broadest endpoint technology platform enables pharmaceutical, biotech, and medical device partners to transform...

Job SummaryWe are seeking a highly skilled Clinical Trial Solutions Specialist to join our team at Clario in Costa Rica.

Job OverviewWe are seeking an experienced clinical research professional to join our team as a Clinical Research Associate II. In this role, you will be responsible for managing clinical trials at various sites, ensuring compliance with regulatory requirements and company policies.Key Responsibilities- Conduct site initiation, monitoring, and close-out...

Job Summary\We are seeking a skilled Clinical Data Specialist to join our team in Costa Rica. This role will involve reviewing clinical trial data, generating and resolving queries, and collaborating with external vendors.\About the Company\Saj Fortrea Costa Rica Srl is a leading contract research organization (CRO) with a strong commitment to scientific...

We are seeking an experienced Clinical Data Management Associate to join our dynamic team at MicroPort Orthopedics Sa. This role will be responsible for overseeing the management of clinical trial data, ensuring accuracy, integrity, and compliance with regulatory requirements.About the RoleThe successful candidate will possess strong analytical skills,...

At MicroPort Orthopedics Sa, we're seeking a skilled Clinical Data Management Associate to join our team. As a key member of our data management group, you'll play a vital role in ensuring the success of our clinical trials.Job Description:As a Clinical Data Management Associate, your primary responsibility will be to manage study start-up tasks, including...

Company Overview: As a leading global contract research organization, Fortrea is dedicated to delivering high-quality clinical development solutions across various therapeutic areas.">About the Role: We are seeking a motivated Clinical Data Specialist to join our team in Costa Rica. This individual will be responsible for conducting clinical data reviews,...

About the RoleWe are seeking a highly skilled Safety Surveillance Associate to join our team at Pfizer. This role will involve reviewing and preparing reports of adverse drug experiences, determining the safety profile of Pfizer's products, and ensuring compliance with regulatory requirements.Key ResponsibilitiesIdentify routine cases for processing,...

Job OverviewServe as a key member of the project team with primary responsibility for clinical data review, query generation and resolution to support the delivery of clinical data according to client quality and integrity specifications.Main ResponsibilitiesReview clinical trial data in accordance with global data management plans and standardized processes...

Company Overview: Fortrea is a leading global contract research organization (CRO) that combines scientific rigor with decades of clinical development experience. With operations in over 90 countries and more than 19,000 staff members, Fortrea provides a wide range of solutions for pharmaceutical, biotechnology, and medical device customers across multiple...

Job SummaryMsd is seeking a skilled Clinical Database Testing Analyst I to join our team. The ideal candidate will have a solid understanding of database design and development, as well as experience with testing and validation of Electronic Data Capture (EDC) systems.ResponsibilitiesPerform execution of standard and trial specific test scripts and record...

About the RoleCurebase is seeking a Quality Engineering Director to lead our efforts in decentralized clinical trials. As a key member of our team, you will be responsible for developing and implementing a vision for quality engineering that aligns with our company's goals.Key ResponsibilitiesDevelop and socialize a compelling roadmap for quality...

Job SummaryAt Msd, we are seeking a skilled Clinical Database Specialist to join our team. The ideal candidate will have a strong understanding of database design and development, as well as experience in testing and validating Electronic Data Capture (EDC) systems.Key ResponsibilitiesExecute standard and trial specific test scripts and record test data and...

About the RoleWe are seeking an experienced Medical Device Safety Specialist to join our team at Microport Orthopedics S.A. in Costa Rica.This is a full-time position that requires strong analytical and problem-solving skills, as well as excellent communication and technical writing abilities.ResponsibilitiesOrganize and conduct Post-Market Surveillance...

We are seeking a Senior Clinical Data Manager to join our team at MSD. In this role, you will be responsible for creating and developing clinical databases and data transfer files according to written specifications.As a Senior Clinical Data Manager, you will lead and participate in the review of electronic case report forms (eCRF) and edit checks, database...

Job SummaryAmazon Support Services Costa Rica Srl is seeking a Trust & Safety Senior Associate (Brazil) to join our Prime Video team. As a key member of our Trust & Safety team, you will be responsible for working with a global team of Policy, Program, Engineering, Legal and other teams to prevent violating content from appearing on PV and ensuring customers...

Company Overview: Clario is a technology company dedicated to transforming the clinical trials industry. Our mission is to put people first, always.Estimated Salary: $60,000 - $80,000 per yearJob Description:Key ResponsibilitiesDeliver superior customer service by providing best business practices and support in using Clario's products for the duration of...

About the RolePfizer is seeking a skilled Safety Data Management Specialist to join our team!The ideal candidate will be responsible for monitoring our drug, biologics, and medical devices surveillance program, including intake, evaluation, and processing of adverse reports. This role will also support clinical trials and post-marketing activities.In this...

Job SummaryThe Safety Data Specialist is responsible for processing adverse experience information in the global safety system for investigational and/or marketed products. Under the direction and supervision of a GPVCM Manager, the Safety Data Specialist performs triage, analysis and interpretation of AE data following our Company Standard Operating...