Clinical Data Management Expert

About the Role:Msd is seeking a skilled Clinical Data Management Analyst to join our team. As a key member of our data management team, you will be responsible for end-to-end data management activities for clinical trials.Key Responsibilities:

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...

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...

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...

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...

Msd seeks an experienced Clinical Data Management Systems Lead to join our team.About the RoleAs a Clinical Data Management Systems Lead, you will be responsible for creating and developing clinical databases and data transfer files according to written specifications. You will lead and participate in the review of electronic case report forms (eCRF) and...

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 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, and project timelines.ResponsibilitiesReview clinical trial data in accordance with standardized data management...

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 OverviewServe as a key member of our global clinical trials team, focusing on clinical data review and query resolution to ensure timely delivery of high-quality data to clients.About the RoleReview clinical trial data in accordance with established data management plans and SOPs to identify errors, missing information, or inconsistencies.Generate,...

Job DescriptionWe are seeking a highly motivated Clinical Data Specialist to join our team at SAJ Fortrea Costa Rica SRL. As a key member of our project team, you will be responsible for clinical data review, query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications, and...

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,...

Msd is seeking a skilled Clinical Data Management Analyst to execute end-to-end data management activities for clinical trials. As a key member of our team, you will be responsible for developing, validating, and maintaining data management tools and systems, ensuring compliance with company Standard Operating Procedures and guidelines.**Job...

Job Summary: We are seeking a highly skilled Clinical Expert Consultant to join our team at Pfizer. As a key member of our Medical Affairs department, you will play a vital role in providing scientific support and strategic insights to drive business growth.About the Role:We are looking for an expert in medical communication who can provide accurate 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...

**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 Us:Msd is a leading pharmaceutical company dedicated to improving lives through innovative medicines and solutions.Compensation:The estimated salary for this role is $130,000 - $180,000 per year, depending on experience and qualifications.Job Summary:We are seeking an experienced Clinical Database Lead to join our team. As a key member of our clinical...

At MSD, we are seeking a highly skilled Clinical Data Integration Specialist to join our team in Costa Rica. This role will be responsible for the operational effectiveness and efficiency of GCDI functions within the geography as well as strategic aspects.The ideal candidate will be a self-directed and self-driven individual who can operate in a Volatile,...

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...

The Straumann Group is a leading provider of innovative solutions for tooth replacement and orthodontic care. We unite global brands to deliver exceptional results in dentistry.As a Clinical Excellence Specialist, you will play a key role in ensuring our customers receive the best possible clinical experience. Your responsibilities will include:Providing...