The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s)...

Responsible for providing Clinical Research support for all clinical trials. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other...

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the SrCRA leads, facilitates and coordinates all clinical trial activit...

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the SrCRA leads, facilitates and coordinates all clinical trial activit...

Assign tasks to Clinical Research Assistants and Clinical Research Associates as appropriate in collaboration with the CRC manager. While the Principal Investigator is primarily responsible for the ov...

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the SrCRA leads, facilitates and coordinates all clinical trial activit...

Assign tasks to Clinical Research Assistants and Clinical Research Associates as appropriate in collaboration with the CRC manager. While the Principal Investigator is primarily responsible for the ov...

Logitech is the Sweet Spot for people who want their actions to have a positive global impact while having the flexibility to do it in their own way.In today's rapidly evolving business landscape, dig...

Logitech is the Sweet Spot for people who want their actions to have a positive global impact while having the flexibility to do it in their own way.In today's rapidly evolving business landscape, dig...

The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s)...

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the SrCRA leads, facilitates and coordinates all clinical trial activit...

Clinical Research; 3 years of experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is required. The Clinical Research Associate is an integral part of...

Clinical Research; 3 years of experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is required. The Clinical Research Associate is an integral part of...

Assign tasks to Clinical Research Assistants and Clinical Research Associates as appropriate in collaboration with the CRC manager. While the Principal Investigator is primarily responsible for the ov...

Assign tasks to Clinical Research Assistants and Clinical Research Associates as appropriate in collaboration with the CRC manager. While the Principal Investigator is primarily responsible for the ov...

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the SrCRA leads, facilitates and coordinates all clinical trial activit...

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the SrCRA leads, facilitates and coordinates all clinical trial activit...

Innova Solutions has a client that is immediately hiring for a.Position type: Full-time, Contract.Work scope will include operati.

Global Pharma company looking to hire experienced Project Manager to join their growing ; This is not an IT ; Must have experience within Pharm.

Global Pharma company looking to hire experienced Project Manager to join their growing ; This is not an IT ; Must have experience within Pharm.

Innova Solutions has a client that is immediately hiring for a.Position type: Full-time, Contract.Work scope will include operati.

Minimum of 8 + years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials. Responsible for c...

Minimum of 8 + years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials. Tracking of clini...

JOB TITLE: Project Coordinator / Jr PM.JOB LOCATION: New York, NY (Park Ave.Minimum Required Qualifications.

JOB TITLE: Project Coordinator / Jr PM.JOB LOCATION: New York, NY (Park Ave.Minimum Required Qualifications.

Responsible for coordination with clinical suppliers to ensure appropriate and timely delivery of clinical trial supplies to clinical sites. Minimum of 8 + years drug development experience in the pha...

Responsible for coordination with clinical suppliers to ensure appropriate and timely delivery of clinical trial supplies to clinical sites. Minimum of 8 + years drug development experience in the pha...

Evidence of continued excellence in clinical practice, such as innovative accomplishments in delivery of care, clinical productivity, and quality improvement initiatives, along with an identifiable ar...

Evidence of continued excellence in clinical practice, such as innovative accomplishments in delivery of care, clinical productivity, and quality improvement initiatives, along with an identifiable ar...

Responsible for providing Clinical Research support for all clinical trials. Participate in the evaluation of potential clinical sites according to established criteria of acceptability. Responsible f...

The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established p...

Independently responsible for the successful management of clinical study sites and monitoring activities for assigned clinical studies of moderate complexity projects. Working knowledge of US (21 CFR...

Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Manager/Specialist, Local Drug Safety Officer (where...

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 development as a Clinical Research Associ...

Columbia Law School seeks an experienced lawyer with a background in criminal defense and a strong interest in community lawyering and clinical teaching to join the Criminal Defense Clinic as the Clin...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. If applicable, may be accountable for site financial management according to executed clinical trial agreem...

The Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice.

Through the above mentioned partnership and an academic appointment at Rutgers, The State University of New Jersey, unique opportunities exist for collaborations between clinical and research programs...

As an Associate Director of Drug Safety and Pharmacovigilance Scientist, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related...