Home based Clinical Research Associate job offers

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

Main purpose of the job:To assist the Site Leader and Principal Investigators in coordinating all aspects of Clinical Trials, including clinic management, staffing, data collection, data storage, quality control, and project management, frequent communication with Study Investigators, Study Coordinators, and the Study teamLocation:Jose Pearson TB Hospital, Gqeberha (Port Elizabeth)Key performance...

The Senior Research and Insights Associate is responsible for providing research expertise, advice, designing solutions and adding value to customers through delivering client-focused, appropriately analysed, data-driven insights and recommendation reporting. The role is also responsible for workshopping solutions and presenting their findings to clients. Client advisory role to proactively addre...

Looking for an experienced Researcher to play a pivotal role in our team. This position offers a unique opportunity for someone,to conduct in depth market research, gather critical insights and contribute to changing people's lives. The suitable candidate will involve conducting deep dives, data, collaborative projects, writing reports.The coordination of diaries and booking appointments.Preparin...

Minimum requirements for the role: Must have minimum a BSc degree in a relevant Agricultural discipline Minimum 2 years hands-on experience in the design and execution of general, field and laboratory trial setups will be required Must have a strong record of innovation and applying modern technology Knowledge of seed production operations will be beneficial Must have excellent communication skil...

Clinical Research Nurse Rheumatology, Cape TownOur client is seeking to recruit an experienced Research Nurse for clinical trials in the Northern Suburbs of Cape Town.The post entails regular contact with volunteers to take part in research that could make a real difference to future rheumatology patient care. This exciting work covers a range of rheumatology studies, looking at new clinical proc...

Main purpose of the job:To assist the Site Leader and Principal Investigators in coordinating all aspects of Clinical Trials, including clinic management, staffing, data collection, data storage, quality control, and project management, frequent communication with Study Investigators, Study Coordinators, and the Study teamLocation:Jose Pearson TB Hospital, Gqeberha (Port Elizabeth)Key performance...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...

Basic Function and Scope of Responsibilities: As an Operations Support Specialist (OSS) you are the frontline support to FPI customers requiring emergency assistance and advice. FPI has a strong set of operational protocols which forms the foundation from which we respond and assist customers in an emergency. The OSS team runs 24/7 and shift work includes nights, weekends, and public holidays.Pri...