Clinical Site Monitoring Specialist

We are seeking a Senior Clinical Research Associate to manage, deliver and/or perform full clinical site monitoring services for one or more projects.Key Responsibilities:Act as primary liaison between CRAs and project teamParticipate in the development of project plans, protocols, CRFs, communications or other monitoring forms, documents and toolsRepresent...

Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document...

Job Title: Clinical Monitoring SpecialistJob Description:The Clinical Monitoring Specialist will perform centralized monitoring activities for clinical research studies in accordance with project plans, protocols, and regulatory requirements. This role involves analyzing site and study level data, identifying risks and trends, and summarizing findings for...

Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document...

We are seeking a Clinical Data Specialist to join our team. The successful candidate will be responsible for providing support to activities related to coding of clinical data for ongoing clinical studies.The ideal candidate will have thorough knowledge of medical terminology and experience working with clinical trials or within the pharmaceutical...

Primarily a training and development role, this position will support and observe clinical site monitoring services both inhouse and in the field whilst developing CRA skills and knowledge. This role will have exposure and training in all aspects of the clinical site monitoring services whilst providing monitoring and site management activities for...

Job DescriptionThe Central Monitor is a vital role in the success of Phase I-IV clinical research and non-interventional studies. Their primary responsibility is to conduct centralized and prompt monitoring activities according to project plans, the protocol, ICH-GCP, and all applicable local and federal regulatory requirements.Key Responsibilities:Review...

**Project Management**: - Manage the planning, execution, progress and completion of assigned clinical research projects. - Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies. - Maintain operational, financial and regulatory integrity and safety. - Develop and/or participate...

**Project Management**:- Manage the planning, execution, progress and completion of assigned clinical research projects.- Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies.- Maintain operational, financial and regulatory integrity and safety.- Develop and/or participate in the...

**Project Management**:- Manage the planning, execution, progress and completion of assigned clinical research projects.- Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies.- Maintain operational, financial and regulatory integrity and safety.- Develop and/or participate in the...