Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...

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...

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...

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...

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...

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)...

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)...

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...

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...

Enters data confirms eligibility register/randomize patient/subject and reports all adverse events to applicable agencies per protocol and internal policy requirements Performs intra operative monitor...

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.

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.

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...

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...

We are seeking an experienced and results-driven Project Manager to oversee the planning, procurement, and implementation of large-scale public safety radio systems.This position will work closely wit...

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...

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...

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...

Job Name:Project Manager & Continuity Expert.Join one of the largest pharmaceutical that is driven by science and seek to push the boundaries of what's possible in m.

Basic competence with methodological approaches and tools in health services research is required, , literature review, clinical data interpretation and claim data analysis. Request: Clinical-Scientif...

Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Generate cl...

Assist with other assigned clinical responsibilities within scope of role to provide best practice and/or support to junior clinical staff. Works with Clinical Trial Oversight Managers (CTOMs) and Cli...

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...

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...

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. If applicable, may be accountable for si...

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

Strong knowledge of Good Clinical Practice (international quality standard for human clinical trials) and local regulations. Clinical Research Associate (CRA) III. As a Clinical Research Associate (CR...

Strong knowledge of Good Clinical Practice (international quality standard for human clinical trials) and local regulations. As a Clinical Research Associate (CRA) III, your responsibilities:. Conduct...