Clinical Data Management Analyst | Expert in Trial Operations

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...

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...

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...

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...

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,...

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...

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,...

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...

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

**Company Overview:** Labcorp is a leading healthcare company dedicated to improving human health. Our organization operates with integrity, respect for people and the environment.As a Clinical Data Analyst at Labcorp, you will play a vital role in ensuring data quality and accuracy. This position involves collaborating with project teams to set up,...

Msd is seeking a highly skilled Clinical Data Management Analyst to join our team. As a key member of our data management department, you will be responsible for executing end-to-end data management activities related to clinical trials.About the Role:The successful candidate will have a bachelor's degree in any field, preferably in health sciences. They...

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...

Job OverviewMsd is seeking a highly skilled Clinical Data Management Analyst to join our team. This role will be responsible for executing end-to-end data management activities for clinical trials, developing and maintaining data management tools and systems, ensuring data integrity through review and reconciliation, and managing queries, medical coding, and...

About the RoleWe are seeking a highly skilled Clinical Trial Hub Safety Associate Professional to join our team at Pfizer. In this role, you will play a critical part in ensuring the safety and efficacy of our pharmaceutical products.Key Responsibilities:Monitor drug, biologics, and medical devices surveillance programs, including intake, evaluation, and...

Job SummaryWe are seeking a highly skilled Clinical Database Testing Analyst I to join our team at Msd. The successful candidate will be responsible for the testing and validation of Electronic Data Capture (EDC) systems.Primary Responsibilities:Perform execution of standard and trial specific test scripts and record test data and test results;Edit check...

**About the Role**We are seeking a highly skilled Clinical Data Operations Manager to join our team at MSD. This is an exciting opportunity for a motivated and experienced professional to lead our clinical data operations functions in Costa Rica.The successful candidate will be responsible for ensuring the operational effectiveness and efficiency of our...

At Msd, we offer a competitive salary of $85,000 to $110,000 per year, depending on location and experience.Job OverviewWe are seeking an experienced Clinical Data Management Specialist to join our team. In this role, you will be responsible for creating and developing clinical databases and data transfer files according to written specifications.About the...

About the Role">Msd is seeking a highly skilled Clinical Data Management Specialist to join our team. This role will be responsible for creating and developing clinical databases and data transfer files, leading and participating in the review of electronic case report forms (eCRF) and edit checks, and reporting deliverables supporting data cleaning and...

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...

Msd is seeking a Clinical Data Management Lead to join our team.Job DescriptionThe Clinical Data Management Lead will be responsible for leading and participating in the review of electronic case report forms (eCRF) and edit checks, database development, programming of edit checks, and scripts to aid in transfer of electronic data files into the Clinical...