Senior Clinical Trial Manager

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

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...

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...

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...

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...

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,...

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 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 RoleWe are seeking a highly skilled Site Manager to join our team at Novasyte. In this role, you will be responsible for managing and monitoring clinical research sites, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.

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 UsOur company, MSD, is a research-driven biopharmaceutical leader that applies its global capabilities to aggressively advance and discover innovative medicines and vaccines. We are dedicated to making a significant impact on the world of healthcare through our commitment to science and by serving the needs of physicians, patients, payers, and other...

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...

**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...

About the RoleWe are seeking a highly skilled Senior Clinical Data Management Systems Lead to join our team at MSD. In this role, you will be responsible for leading the development and implementation of clinical data management systems, ensuring that they meet the highest standards of quality and regulatory compliance.Key ResponsibilitiesLeverage your...

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...

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...