Clinical Research - Miami

We are seeking a dedicated and detail-oriented experienced Travel Clinical Research Coordinator to join our team. · In this role, you will be responsible for overseeing clinical trials at different sites and ensuring compliance with regulatory standards.Coordinate and manage all ...

We're shaping the future of community clinical research by being the partner of choice for CROs, Sponsors, and PIs. · ...

We are seeking a Clinical Research Coordinator to join our team and play a key role in managing clinical studies across multiple therapeutic areas. · This position is ideal for an organized driven professional who thrives in a collaborative research environment.Gain thorough know ...

We are seeking a Clinical Research Coordinator to join our team. · Gain thorough knowledge of study protocols in collaboration with the Principal Investigator (PI) and Site Director prior to study activation · Develop, review, and refine source documents before study launch · ...

+Job summary · Clinical Research Regulatory Coordinator facilitates site operations and assists in the development of the Rovia network. · +Manages site selection visits and coordinates study startup activities. · Oversees facility issues in collaboration with the Site Manager an ...

The Clinical Research Coordinator facilitates site operations and assists in the development of the Rovia network, including planning, coordinating and executing clinical studies in accordance with the protocol, · Manages site selection visits and coordinates study startup activi ...

The Regulatory Specialist will maintain day-to-day regulatory tasks within the site network and assist with clinical studies in accordance with protocol. · ResponsibilitiesPerforms startup activities including IRB submissions. · Assists with management of eRegulatory platform Com ...

The Clinical Research Coordinator works in collaboration with other members of the clinical research site team to ensure execution of assigned studies in compliance with regulations. · ...

Alcanza Clinical Research is a national collaborative network of clinical research sites founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all. · ...

We are looking for a Clinical Research Coordinator to join our team at Alcanza, a growing multi-site clinical research company with locations across the US. · ...

+Job summary+Join us as we continue to grow. · +Qualifications+A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience · ...

We are launching a new community-based clinical research site embedded within an established internal medicine and geriatric practice.We seek an experienced Clinical Research Coordinator to help launch and build this site. · ...

Join Alcanza Clinical Research as a Clinical Research Coordinator and contribute to the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. · ...

The Clinical Research Medical Assistant assists with the execution of new studies and maintains open and closed studies performing administrative and clinical tasks for trials. · Required Skills/AbilitiesSound knowledge of medical terminology. · Sound knowledge of ICH/GCP and Reg ...

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, · GA, IL, · M A · ,MI,M O,NV ,SC,TX, · V A and Puerto Rico. · The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance ...

To work as an integral member of the Rovia/Investigator site staff, maintaining day-to-day operations and assist in development of Rovia network. · ...

To work as an integral member of the Rovia/Investigator site staff, maintaining the day-to-day operations and assist in the development of the Rovia network. · ...

We are seeking a dynamic and detail-oriented Clinical Research Recruitment Coordinator to join our innovative research team. In this role, you will be the vital link between clinical trial participants and our research objectives, ensuring seamless recruitment, engagement, and co ...

This Clinical Research Coordinator role involves managing day-to-day clinical trials processes in Fort Lauderdale, FL. · ...

Clinical research source writer responsible for creating all source documentation needed for clinical trials. · ...

The Clinical Research Principal Investigator oversees the entire research process, ensures participant safety and compliance with regulations, and identifies participants for clinical studies. · Oversight and Technical Success: The PI ensures the project's technical success, foll ...