Senior Clinical Research Manager

Senior Clinical Research CoordinatorClinical Research Associates with experience in site management and monitoring are needed to coordinate and manage clinical trials. The ideal candidate will have excellent communication and organizational skills, as well as the ability to work effectively in a team environment.ResponsibilitiesSite Coordination and...

Participates in designing and executing clinical research tasksrequired for research and/or clinical protocols; coordinates and participatesin a variety of complex activities involved in the collection, compilation,documentation and analysis of clinical research data under the direction of aPrincipal Investigator or Project Leader. **Essential...

Responsible for increasing the quality and quantity ofclinical research performed in the Department and therefore promote anatmosphere of serious enquiry among all members of the department especially thejunior staff. **Essential Responsibilities and Duties**: 1. Maintains an updated log book of all approved clinical research protocols stating the dates of...

Participates in designing and executing clinical research tasks required for research and/or clinical protocols; coordinates and participates in various complex activities involved in collecting, compiling, documenting, and analyzing clinical research data under the direction of a Principal Investigator or Project Leader. **Essential Responsibilities and...

**Clinical Research Associate (level dependent on experience)** **Job Purpose/Summary** As a CRA you will be responsible for the successful conduct of clinical trials and serve as the main contact for the investigative site by representing CTI in a professional manner. **What You’ll Do** - Conduct evaluation, initiation, monitoring and close out...

**Clinical Research Associate (level dependent on experience)** **Job Purpose/Summary** As a CRA you will be responsible for the successful conduct of clinical trials and serve as the main contact for the investigative site by representing CTI in a professional manner. **What You’ll Do** - Conduct evaluation, initiation, monitoring and close out...

Job DescriptionKing Faisal Specialist Hospital & Research Centre (Gen. Org.) is seeking a highly skilled Clinical Research Professional to join our team. The ideal candidate will participate in designing and executing clinical research tasks, ensuring compliance with protocols and objectives.Main Responsibilities:Design and execute clinical research...

About the RoleThis position involves collaborating with department heads and clinical research staff on clinical and research programs/projects. Key responsibilities include advising on scientific and clinical approaches, supporting clinical research and technical staff, participating in research proposal development, and communicating results through...

**Company Overview**At CTI Clinical Trial and Consulting Services, we strive to be a leader in the clinical trials industry. Our team is passionate about making a difference in the lives of patients by bringing life-changing therapies to market.

Assists and coordinates clinical research daily tasks required for research and/orclinical protocol; assists in a variety of complex activities involved in thecollection, compilation, documentation and analysis of clinical research dataunder the direction of a Principal Investigator or Project Leader. **Essential Responsibilities and Duties**: 1. Assists in...

Job Title: Clinical Research AssistantAbout the Role:We are seeking a highly skilled Clinical Research Assistant to join our team at King Faisal Specialist Hospital & Research Centre. As a Clinical Research Assistant, you will be responsible for conducting laboratory tests and experiments, maintaining laboratory equipment, and ensuring compliance with safety...

We are seeking a talented Clinical Research Assistant to join our team at Nahdi. As a Clinical Research Assistant, you will play a vital role in supporting the development and implementation of clinical research projects.Duties and ResponsibilitiesAssisting in the preparation and conduct of clinical trials and studies.Coordinating with researchers,...

CARE is committed to providing exceptional patient care and outcomes through innovative medical treatments. As part of our clinical research team, you will contribute to this mission by serving as a Clinical Research Data Manager.Main DutiesServe as Data Team Lead on a program of 6-10 global clinical trials or 40+ increasingly complex central laboratory...

Responsible for the management of clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation (Protocols, Case report forms, Investigators brochures, Consent documents, Letters of Agreement, Confidentiality Agreements), organizing trial related regulatory submissions with follow-up...

Responsible for the management of clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation (Protocols, Case report forms, Investigators brochures, Consent documents, Letters of Agreement, Confidentiality Agreements), organizing trial related regulatory submissions with follow-up...

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance, liaise with vendors; and other duties, as assigned - Responsible for aspects of registry management as prescribed in the project plans - General...

Supervises and provides leadership to medical technology service teams, within the Clinical Engineering Department, that provide for the operational and technical support od medical diagnostic, therapeutic and analytical devices and systems, utilized for applied patient healthcare and healthcare research. Acts as the senior operational and technical resource...

Role Purpose The Clinical Research Coordinator (“CRC”) comprises an integral part of the research team at the Sites level. Working in coordination with the Principal Investigator, he/she is responsible to support the Principal Investigator in conducting the Study in accordance with ICH-GCP, regulatory standards, Protocol study design and client...

**Role Purpose**: **The Clinical Research Coordinator (“CRC”) comprises an integral part of the research team at the Sites level. Working in coordination with the Principal Investigator, he/she is responsible to support the Principal Investigator in conducting the Study in accordance with ICH-GCP, regulatory standards, Protocol study design and client...

About the Job">As a Clinical Research Associate at IQVIA, you will play a critical role in ensuring the successful execution of clinical trials. Your primary responsibility will be to conduct site monitoring visits and provide support to study sites to ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and sponsor requirements.Key...