Clinical Trial Assistant, TMF - United States of America

We are seeking a TMF Quality & Oversight Specialist to support the review, quality oversight, and maintenance of Trial Master File (TMF) documentation in accordance with GCP, ICH E6, regulatory requirements, and 4DMT SOPs. · Perform detailed QC reviews of TMF documents to verify ...

We're seeking an experienced TMF Records Specialist (TRS) to join our sponsor-dedicated team. · <ul style=\ ...

Clinical Document Specialist · 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 de ...

Clinical Document SpecialistICON 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 devel ...

4DMT seeks a motivated and experienced Senior Clinical Trial Associate to support the Company's clinical trial activities. · ...

The Study Start-Up Manager is accountable for study planning, SSU activities and activation deliverables of assigned projects in compliance with client processes, GCP/ICH and regulatory requirements in a standalone country, · OPC (operating country) or satellite country. · ...

· Relocation Assistance Offered Within Country · # Piscataway, New Jersey, United States · Candidates seeking this position will be based at the Colgate-Palmolive Global Technology Center located in Piscataway, NJ. The candidate's main duties will involve conducting clinical stu ...

We are a small biotechnology company focused on advancing novel therapies to address serious unmet medical needs. This role offers an excellent opportunity to gain broad exposure to clinical trial execution in a fast-paced startup environment. · Provide administrative and operati ...

The Senior Manager, Clinical Quality Assurance (CQA) provides comprehensive technical support and expertise in risk-based quality management of clinical trials. · ...

Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers direct ...

BrainChild Bio, Inc. is seeking a motivated and detail driven Clinical Research Associate (CRA) to support the execution and monitoring of our CAR T clinical trials. · ...

We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with but make us easier to work for. · ...

Description · Principal CRM & Digital Solutions Presales Architect  - Communications · Description · Oracle Communications Sales Consulting focuses on delivering strategic solutions for customers in the Communications Industry.  Specifically, our team supports our customer's digi ...

Description · With ongoing and ground-breaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to join ...

RTI International is seeking a Lead Clinical Study Manager (Lead CSM) to join our team. The ideal candidate will be highly motivated, results-oriented, and collaborative with experience leading multi-site clinical trial operations and drug development initiatives. · ...

Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · ...