Clinical Study Administrator

Join **RAY CRO** as a Clinical Study Coordinator! We're seeking motivated individuals in Riyadh to contribute to advancing medical research. As a Coordinator, you'll oversee study activities, collaborate with investigators, and ensure protocol adherence. **Qualifications**: - Bachelor's degree in a relevant field. - Previous clinical study coordination...

**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...

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...

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...

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...

**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...

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...

**Essential Functions and Other Job Information** 1. Maintaining personnel documents and files, both on paper and electronic as authorized by HR Associate 2. Maintenance of HR databases and supportive tools and systems 3. Participation in the internal meetings 4. Assisting in preparation of any forms, announcements and logs necessary for daily activities...

**Clinic Manager** is required for a very reputable Clinic located in **Riyadh**/Saudi Arabia to ensure efficiency and excellence in service delivery. ▪︎Work closely with medical professionals and administrative staff to enhance clinic services .▪︎Minimum of 5 years of experience in managing medical clinics, with a proven track record of successful...

**Contract type**: Full Time - Permanent **Location**: Riyadh, Saudi Arabia Study Group is looking for a dynamic Partnership and Business Development Manager to drive sustainable and commercially viable partnerships in both B2B and B2G sectors across the Middle East. This role involves leading the development of strategic alliances, expanding our market...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

**Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Essential Functions** - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in...

Clinical Research Associate **Category**:Clinical Development**Location**:Riyadh, Riyadh, SA- Are you a dedicated clinical trial professional with direct site management experience? Are you highly motivated by being able to make a difference in improving patients’ lives? If yes, keep reading - this role might be just for you!- Novo Nordisk is on the...

Plans and manages patient-related research projects independently within a specifically defined field of study, but typically part of a clinical research program; analyses science-driven clinical studies; participates in writing papers and proposals; and supervises students and trainees. **Essential Responsibilities and Duties**: 2. Executes the results of...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

**Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Essential Functions** - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in...

**Clinical Psychologist** **We are hiring for A Medical Center In Saudi Arabia (Riyadh & Dammam) a "Clinical Psychologist"** **Main Details;** - **Full Time job - Onsite** - **Open for Any nationality yet must speak English fluently** - **Age is not more than 45 Years Old** - **Package is negotiable** - **Preferable HAVE EARNED HIS/HER DEGREE / TRAINING...

Cochlear is the global market leader in implant hearing solutions. Cochlear's mission is to help people hear and be heard. Around the world, more people chose a Cochlear-branded hearing implant system than any other. A Cochlear Implant is an electronic device that is surgically implanted under the skin near the ear that restores hearing to those who suffer...

**Job Purpose**: The clinic manager is responsible for the management and daily operations of the assigned Skin Laundry clinic. The clinic manager ensures that staff are following the established policies & procedures for client journey, managing the medical and administrative team members, and achieving business goals. She must keep track of the revenue and...