Senior Clinical Trial Coordinator- España

If you are an experienced **Clinical Trial Manager **who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial...

Senior Clinical Trial Managers at Parexel FSP play a pivotal role in supporting, coordinating, and delivering our clients’ regional and global clinical trials. This includes full involvement in study start-up, maintenance, and close-out, as well as vendor management and CRA oversight. If you’re a Senior CTM with experience of these activities, we can...

Parexel are currently recruiting for an experienced Oncology Associate Clinical Trial Manager. In this position you will be the individual responsible for the coordination of clinical operations required to initiate, execute and complete clinical trials to drive on-time delivery of clinical trial milestones. May act in support or lead role **Some specifics...

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development...

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator. This part-time (20 hours) role, is planned for 11 months and is to support the site in** El Palmar, Murcia** in conducting a clinical trial in the field of...

Within this role, you will be responsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities to ensure compliance with SOPs, GCP and regulatory requirements. You will also engage with clinical sites to develop, build, and maintain strong...

In Parexel FSP we are looking for a Senior Clinical Contracts Analyst based in Spain. **Position Purpose**: The Senior Clinical Contract Analyst serves as a conduit between Clinical Operations and the Legal group for contract requests including Confidentiality Agreements, Clinical Trial Agreements (CTAs), Ancillary Services Agreements, Consultant Agreements...

**Job summary**: As an experienced **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and...

Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added...

Additional Job Description The **Initiation Clinical Research Associate II **(**iCRA II**) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA II can also support...

These customers have new therapeutic ideas, but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You’ll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you’ll help make a positive difference in...

The **Initiation Clinical Research Associate II **(**iCRA II**) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA II can also support protocol amendments if...

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction. As a CRA...

You will be supporting a long-term partnership with one of the most established pharmaceutical companies in the industry. Within this program you will find a culture focused on teamwork and camaraderie; where every member plays an integral part. You will have the opportunity to work on breakthrough technologies in the areas of cardiovascular, oncology,...

Job Overview Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with...

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction. As a CRA...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

Competitive - Milan, Spain - Permanent CRA II/ Senior Clinical Research Associate - Midsized CRO - Remote - Spain - CRA II/ SCRA - Fascinating projects and therapeutic area exposure - Fast progression due to tailored training programmes - Excellent work environment Company Background: Opportunity to join a full-service CRO with offices spanning six...

Additional Job Description The **Initiation Clinical Research Associate II **(**iCRA II**) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA II can also support...

ICON has an exciting new opportunity for a Global Project Manager to join a growing and successful team. This is a home-based and permanent role. Key Responsibilities: Responsible for: - Lead the development of realistic study timelines, from design through final study reporting Maintaining accuracy of clinical study timeline information in data control...