Clinical Trial Psych Rater

Clinical Research Manager Job Description About the Role The Clinical Trial Manager will oversee clinical monitoring staff, ensuring trial compliance with project goals. They will create and implement study-specific clinical monitoring tools and documents. Main Responsibilities Collaborate with Project Managers to set targets for clinical monitoring staff....

Job OpportunityA seasoned Clinical Research Specialist is required to oversee trial protocols, establish and manage clinical sites, train staff on therapeutic areas, and ensure compliance with regulatory standards.Key Responsibilities:Develop and execute trial protocols for steering committeesIdentify, evaluate, and set up clinical trial sitesTrain site...

Clinical Research AssociateJob Description:We are seeking a highly skilled Clinical Research Associate to join our team. The successful candidate will be responsible for managing clinical trials from start to finish, ensuring that all trials are conducted in accordance with Good Clinical Practice (GCP) guidelines and regulatory...

JOB DETAILS 1.Creating and writing trial protocols, and presenting these to steering committee.2.Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3.Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4.Liaise with ethics committee...

TMF Specialist Job OverviewWe are seeking a highly skilled professional to fill the role of TMF Specialist within our Clinical Operations group. This position will play a vital part in ensuring the seamless execution of clinical trials, collaborating closely with cross-functional teams.Key Responsibilities:Process study documents in accordance with client...

Clinical Research Associate RoleJob Summary:We are seeking a skilled Clinical Research Associate to join our team. The ideal candidate will have experience in managing clinical trials, ensuring compliance with regulatory requirements, and providing high-quality support to investigators.Responsibilities:Conduct site initiation visits, monitor study progress,...

Age limit:20 to 30.Clinical Study Design & Execution: Leading the design and implementation of clinical study protocols and monitoring their progress.Regulatory Compliance: Ensuring all activities, from clinical trials to post-market evaluations, adhere to regulatory requirements and guidelines (e.g., FDA regulations, GCP).Data Management & Analysis:...

Clinical Research Associate JobWe are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for writing drug trial methodologies, identifying and briefing appropriate trial investigators, setting up and disbanding trial study centres, designing trial materials, providing clinicians...

Clinical Trial Manager RoleWe are seeking a senior clinical research associate to ensure the smooth conduct of clinical trials. Their role involves collaborating with project managers to set targets, creating and implementing study-specific tools and documents, and overseeing trial activities.The ideal candidate will have experience in clinical research,...

Job descriptionRole & responsibilities:Overseeing the collection, validation and processing of clinical trial data.Developing and implementing data management procedures for clinical trials.Supporting and facilitating the review of medical coding for validity and completeness.Ensuring compliance with applicable regulations, protocols and standard operating...