Key Responsibilities:Provide oversight of clinical development with input on global strategyInterpret and communicate clinical trial dataIdentify new clinical research opportunities and support in-licensing and out-licensing activitiesRequired Qualifications:MD or DO degree from an accredited medica...
Apsida Life Science have partnered with a leading CRO who are looking for a CRC (Clinical Research Coordinator). ...
A company is looking for a Clinical Research Coordinator for a Clinical Trials Processing Lab. ...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 3 years’ experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH g...
Key Responsibilities:Oversee operational strategy, planning, risk assessment, and execution of observational research studiesManage people, career development, and training of team members supporting the Observational Research PortfolioCoordinate audit and inspection activities, ensuring compliance ...
Barrington James is looking for Clinical Research Coordinators in multiple locations within Michigan to join our client. This is a 3 month contract opportunity, this is a great opportunity to build a professional relationship with the client and to grow into other positions within the Clinical Resea...
The Clinical Research Coordinator provides research coordination support for multiple clinical research projects. The position involves coordinating various clinical research projects, such as registries, retrospective data reviews, long-term follow-up studies, and other non-interventional studies. ...
Clinical research certification preferred. Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support andguidance in the clinical trials arena. ...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
Unblinded Clinical Research Coordinator I DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Interpret clinic schedule a...
Under the supervision of the investigator(s) and research coordinator, and following established policies and procedures, performs a variety of clinical research activities, and participates in carrying out research objectives, ensuring compliance with all legal, regulatory and protocol guidelines. ...
The Columbia Center for Translational Immunology (CCTI) at Columbia University Irving Medical Center (CUIMC) is actively seeking a dynamic and proficient Clinical Research Coordinator to bolster our research endeavors. Participate in clinical transplant meetings, collaborating with clinical and rese...
Clinical Research Coordinator I The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Liaising with Laboratory team...
The Clinical Research Coordinator (CRC) will be responsible for managing the day-to-day activities of a highly innovative portfolio involving participant engagement in cardiovascular and hypertension clinical research. We are an innovative research entity within the Division of Cardiology (Hypertens...
The Clinical Research Nurse promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. Scope of WorkThe Clinical Research Nurse is responsible for pr...
The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values. Profound enables community physicians to offer clinical research a...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...
POSITION PURPOSE Coordinate and participate in clinical research studies by performing activities involved in the collection, compilation, documentation of research data. The position will work with principal investigators and other research team members to accurately and efficiently carry out a ran...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values. Profound enables community physicians to offer clinical research a...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Clinical Research Professional or Association of Clinical Research Professionals (ACRP) required for a minimum of 12 months prior to assuming CRC IV role. Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Bachel...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...