Clinical Operations Associate

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...

At BeiGene, we are committed to growing our team with experienced professionals who share our passion for fighting cancer. As a Clinical Operations Associate, you will play a critical role in supporting our study teams with Clinical Operations tasks, ensuring compliance, and maintaining the Trial Master File (TMF).Key Responsibilities:Support Clinical...

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...

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 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,...

About the RoleParexel is seeking a Clinical Research Associate II to join our Clinical Operations Team in Spain. This role can be office-based in Madrid or decentralized in the regions of Madrid or Barcelona.As a Clinical Research Associate II, you will be responsible for conducting qualification visits, site initiation visits, monitoring visits, and...

BeiGene is seeking a skilled Clinical Operations Coordinator to support our study teams with clinical trial management tasks.Key Responsibilities:Support cross-functional clinical study teams from start-up through close-outAssist in development of clinical trial documents, manuals, and trackersMaintain clinical operations tracking tools and prepare...

About the RoleParexel is seeking a Clinical Research Associate II to join our Clinical Operations Team in Spain. This role can be office-based in Madrid or decentralized in the regions of Madrid or Barcelona.Key ResponsibilitiesConduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites and...

About the RoleParexel is a global leader in clinical research and development, working with clients across the globe to transform scientific discoveries into new treatments. We are currently seeking a highly skilled Clinical Research Associate II to join our Clinical Operations Team in Spain.Job SummaryThe successful candidate will be responsible for...

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...

Job SummaryWe are seeking a highly motivated and detail-oriented Business Development Associate to join our team in Madrid, ES. As a Business Development Associate - Clinical Event Coordinator, you will play a critical role in supporting the growth and development of our business by coordinating clinical events and projects.Key ResponsibilitiesDevelop and...

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...

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...

About the RoleParexel is seeking an experienced Clinical Research Associate to join our team in Madrid or Barcelona, Spain. As a Clinical Research Associate - Study Start Up Specialist, you will be responsible for performing all study start up activities for clinical trials.Key ResponsibilitiesAct as Parexel's direct point of contact with assigned sites,...

Parexel Site Contract Associate OpportunitiesParexel is a leading provider of biopharmaceutical services, dedicated to transforming scientific discoveries into new treatments. As a Site Contract Associate, you will play a vital role in the negotiation of study-specific clinical site agreements with sponsors, ensuring that our clients' needs are met while...

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 BeiGene:BeiGene is a global biotechnology company that is dedicated to developing innovative cancer therapies and improving the lives of patients worldwide. We are committed to advancing our research and development capabilities, expanding our pipeline of first-in-class and best-in-class candidates, and delivering high-quality products to meet the...

Job SummaryThe Clinical Contract Professional will play a key role in the supervision of administration and negotiation processes for clinical site contracts, ensuring final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal & and regulatory requirements.Main ResponsibilitiesOversight of planning,...

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...

Unlock Your Potential with ParexelThe Client Relationship Director FSP - Enterprise Accounts will be a key member of our Commercial Operations team, working closely with SBU Delivery, Solutions Consultants, and Clients and Partners to drive business growth and success.Identify, target, and secure new business opportunities across Parexel's FSP services,...