Clinical Trial Site Operations Specialist

Job Title: Regional Clinical Trial Management AssociateBeiGene is a rapidly growing company with exciting opportunities for experienced professionals. We are seeking a highly motivated and collaborative Regional Clinical Trial Management Associate to support our Clinical Operations team.Job Summary:The Regional Clinical Trial Management Associate will...

Job Title: Regional Clinical Trial Management AssociateBeiGene is a rapidly growing company with exciting opportunities for experienced professionals. We are seeking a highly motivated and collaborative Regional Clinical Trial Management Associate to support our Clinical Operations team.Job Summary:The Regional Clinical Trial Management Associate will...

Job Title: Regional Clinical Trial Management AssociateJob Summary:BeiGene is seeking a highly motivated and detail-oriented Regional Clinical Trial Management Associate to support the clinical operations team. The successful candidate will be responsible for coordinating and managing clinical trials, ensuring compliance with regulatory requirements, and...

Job Title: Regional Clinical Trial Management AssociateJob Summary:BeiGene is seeking a highly motivated and detail-oriented Regional Clinical Trial Management Associate to support the clinical operations team. The successful candidate will be responsible for coordinating and managing clinical trials, ensuring compliance with regulatory requirements, and...

Clinical Operations Associate Job DescriptionBeiGene is a rapidly growing company with exciting opportunities for experienced professionals. Our team is passionate about fighting cancer and is seeking a highly motivated and collaborative Clinical Operations Associate to support our clinical operations tasks.Responsibilities:Support clinical study teams with...

BeiGene is a rapidly growing company with exciting opportunities for experienced professionals. We are looking for highly motivated, collaborative, and passionate individuals who share our interest in fighting cancer.Job Summary:The Regional Clinical Trial Management Associate will support the study team with Clinical Operations tasks, ensuring compliance...

Job Summary:BeiGene is seeking a highly motivated Clinical Operations Associate to support our clinical trial teams. The ideal candidate will have a strong understanding of clinical operations and be able to work effectively in a fast-paced environment.Key Responsibilities: Assist in the development of clinical trial documents and manuals Prepare and...

BeiGene is committed to advancing cancer treatment through innovative clinical trials. We are seeking a highly motivated and detail-oriented Clinical Operations Associate to join our team.Key Responsibilities:Support clinical study teams with trial management tasks, ensuring compliance with ICH/GCP guidelines and local regulations.Develop and maintain...

Job DescriptionBeiGene is seeking a highly motivated and organized Regional Clinical Trial Management Associate to support our clinical operations team. As a key member of our team, you will play a critical role in ensuring the success of our clinical trials.Key ResponsibilitiesSupport clinical operations tasks, including trial master file (TMF) setup,...

Clinical Operations at ParexelAre you passionate about delivering real impact in oncology studies? We are seeking a Site Monitor to strengthen our clinical operations team in Spain, specifically in Madrid or Barcelona. As a Site Monitor, you will work independently to set up and oversee studies, complete status reports, and maintain documentation. This role...

About the RoleParexel FSP is seeking a highly motivated and experienced Site Monitor to join our clinical operations team in Spain (Madrid or Barcelona). As a Site Monitor, you will play a critical role in ensuring the successful execution of clinical studies, working closely with our team to deliver high-quality results.Key ResponsibilitiesSet up and...

Join Our Team as a Site Monitor in SpainParexel FSP is a leading clinical research organization that values its team members and their dedication to excellence. We are seeking a highly motivated and detail-oriented Site Monitor to join our clinical operations team in Spain, specifically in Madrid or Barcelona.About the RoleAs a Site Monitor, you will work...

Join Our Team as a Site Monitor in SpainParexel FSP is a leading clinical research organization that values its team members and their dedication to excellence. We are seeking a highly motivated and detail-oriented Site Monitor to join our clinical operations team in Spain, specifically in Madrid or Barcelona.About the RoleAs a Site Monitor, you will work...

Parexel FSP: A Leader in Clinical OperationsWhy Choose Us?We are one of only three CROs to have received the Leadership Award for 11 consecutive years. Our team's dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do.About the RoleWe are seeking a Site Monitor in...

The Initiation Clinical Research Associate II (iCRA II) plays a pivotal role in the clinical trial process, specializing in performing all study start-up activities.Key responsibilities include participating in Pre SIV activities, managing and driving the strategy for Pre SIV / start-up tasks, and supporting protocol amendments if applicable.This role...

Study Start-Up SpecialistParexel is seeking a highly skilled Study Start-Up Specialist to join our team. As a key member of our clinical research team, you will be responsible for performing all study start-up activities for clinical trials.Key Responsibilities:Start-Up (from site identification through pre-initiation)Act as Parexel's direct point of contact...

About the RoleParexel FSP is seeking a skilled Site Monitor to join our clinical operations team in Spain (Madrid or Barcelona). As a Site Monitor, you will work independently to set up and oversee studies, complete study status reports, and maintain study documentation.Key ResponsibilitiesParticipate in the submission of protocols, consent documents for...

About the RoleParexel FSP is seeking a skilled Site Monitor to join our clinical operations team in Spain (Madrid or Barcelona). As a Site Monitor, you will work independently to set up and oversee studies, complete study status reports, and maintain study documentation.Key ResponsibilitiesParticipate in the submission of protocols, consent documents for...

We are seeking a skilled professional to join our team at Parexel, a leading biopharmaceutical services company. As a Global Site Contracts Lead, you will play a critical role in negotiating study-specific generic and country Clinical Site Agreement (CSA) templates with sponsors.The ideal candidate will have excellent negotiation skills, a deep understanding...

### Job Title: Patient Data Specialist ### Job Summary: We are seeking a highly skilled Patient Data Specialist to join our team at Precision Medicine Group. As a Patient Data Specialist, you will play a critical role in ensuring the accuracy and quality of clinical trial data. Your expertise in oncology and clinical trials will be essential in reviewing...