Clinical trials jobs in Basingstoke, Hampshire

 ...Experienced UK-based Regional CRA/clinical research associate required to augment existing CRA team, for multinational biopharmaceutical company partner.   You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading... 

 ...Join Us on Our Mission to Drive Healthcare Forward As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical...  ...work-life balance while contributing to cutting-edge clinical trials. Why IQVIA? IQVIA is recognized as #1 in its category on... 

 ...CRA II ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment...  ...will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the... 

 ...out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track subject...  ...originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (... 

 ...Dedicated ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive...  ...you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory... 

 ...Contract ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive...  ...supporting In-house CRA activities relating to the running of Clinical Trials as defined by the study budget Providing support to our... 

Senior Project Associate - Hiring ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of... 

 ...home-based, UK, Slovakia, Romania, Hungary, Bulgaria The Global CPM (Senior Study Leader) is the leader of the cross-functional clinical trial team (CTT), who guides planning and management of the assigned clinical study/studies end-to-end to achieve objectives.... 

 ...Collaborate with multi-disciplinary project teams to establish project objectives and timelines. • Write the statistical sections of clinical trial protocols, while consulting with internal and external experts. • Write statistical analysis plans. • Monitor internal and... 

 ...management activities in support of Client's studies across all stages of clinical drug development. Summary of Key Responsibilities...  ...design/build of an EDC data management system and other Clinical Trial/Data Management Systems Knowledge and understanding of regulations... 

 ...IQVIA is recruiting for a Clinical Specialist to work across London. In this role you will be responsible for maintaining an existing customer base and developing sales in strategic accounts across several UK sales territories. You will become an integral part of the... 

 ...Clinical Registry Administrator role : Provides clinical registry support, oversight and/or accountability for one or more clinical trials. Gathers content and integration requirements for registration records - Establishes expectations for dataset content and structure... 

 ...pharmacy service. • Accurate labelling, dispensing and checking a wide range of prescription types including controlled drugs, clinical trials, total parenteral nutrition, chemotherapy, home IV and palliative care. • Medicines management rotations will allow direct patient... 

IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the medical product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into... 

 ...as needed. The Coder will collaborate with medical monitors, Clinical and Data Management team members, as required, to ensure the timely...  ...WHODD ~ Working knowledge of medical terminology, clinical trials & coding is essential. ~ Excellent written and oral skills and... 

 ...Patient Recruitment Lead- Global Clinical Trial campaigns ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission... 

 ...Clinical Operations Manager - Sponsor Dedicated ICON plc is a world-leading healthcare intelligence and clinical research organization....  ...will play a pivotal role in overseeing the execution of clinical trials, ensuring that they are conducted efficiently, on time, and in compliance... 

 ...organization and the external medical community. By leveraging deep clinical and diagnostic expertise-particularly in the pre-analytical phase...  ...Assist with Investigator Sponsored Studies and identify clinical trial sites and investigators. Cross-Functional Collaboration :... 

 ...Teleradiology Systems Specialist About TMC Telemedicine Clinic (TMC) pioneered teleradiology services in Europe when it was founded in 2002 and has since become a vital partner for more than 120 radiology departments in the UK, Sweden, Denmark, and Norway. In November 20... 

 ...between Monday and Friday, with shifts typically between 7:30am and 5:30pm. However, weekend work may occasionally be required based on clinical activity and service needs. There are also opportunities to travel to other sites to attend training or to support clinical activity... 

Cpl UK Healthcare (formally RIG Locums) are currently looking for an experienced CAMHS Consultant or Associate Specialist in the community service, around Basingstoke. Job Description available with timetable upon request. Job title: Consultant or Associate Specialist...

 ...based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment...  ...Scientist you will be working mostly with the ICON Clinical Trial Units in the Netherlands and Hungary. You will be responsible for... 

 ...Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive...  ...strategies to enhance patient recruitment and retention in clinical trials. You will work closely with cross-functional teams to ensure that... 

 ...Talent Acquisition Team Lead ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical... 

 ...Senior Director DMPK – Nonclinical Consulting ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the... 

 ...Senior SAS Programmer I - EMEA Remote or Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape... 

 ...Psychometrics United Kingdom and Europe Job Overview Real world evidence (RWE) has become a vital complement to the traditional clinical trial in the demonstration of the value and safety of new medicines. This data analyst role sits within our Real World Solutions team... 

 ...offering the opportunity to work on late-phase global oncology trials , with a focus on hematology and regulatory submissions ....  ...Statistics , or a related field. ~5+ years of experience in clinical trials, with a strong focus on oncology (hematology and late-phase... 

 ...client. Sponsorship is not available for this opportunity. #LI-DNI #LI-CES #LI-WS1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent... 

 ...Execute clinical studies/projects/activities and meet planned deliverables in line with agreed and defined roles and responsibilities. Support set-up and maintenance of information in Clinical Trial Management Systems (CTMS) and other systems as applicable, independent...