Jobs: clinical trial manager

**Position Description** **Job Title**:Senior Clinical Trial Manager **Location**: Cape Town, South Africa, Nairobi, Kenya, or Uganda **Reports to**: Associate Director, Clinical Operations **Position Summary**: Help IAVI translate science into global health impact as a Senior Clinical Trial Manager IAVI is seeking a highly motivated Senior Clinical...

Duties/Pligte The Clinical Trial Coordinator will primarily be responsible for the operational oversight and execution of a multi-site prehospital clinical trial at one of two Coordinating Study Units (CSU) within the Western Cape. S/he will support the Clinical Trial Project Manager and Trial Coordinator in ensuring effective execution of this...

ICON plc’s job vacancy, Career and Recruitment Job title : Local Clinical Trial Manager jobs in Gauteng Job Location : Gauteng, Johannesburg Deadline : April 26, 2024 Quick Recommended LinksJobs by Location Job by industries The role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study within Italy . The CTM...

**About SubjectWell**: SubjectWell is a venture-backed technology startup on an unstoppable mission to disrupt patient recruitment for clinical trials, a $100 billion dollar sector. Clinical trials need millions of qualified patient volunteers, but regularly fall behind schedule because patients are unaware of the benefits of clinical trials or even how to...

**Overview**: **Reference** DTHF/C025 **Salary** not applicable **Job Location**: - South Africa - City of Cape Town **Job Type** Permanent **Posted** Friday, April 12, 2024 **Closing date** 26 Apr 2024 23:59 **CLINICAL TRIALS UNIT MANAGER** **PERMANENT** **J52, GROOTE SCHUUR, OBSERVATORY (ON-SITE)** **The Desmond Tutu Health Foundation (DTHF) is a...

**Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution,...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

**About the Company**: TASK is a South African headquartered, multinational clinical research institute that conducts clinical trials to determine the treatment effects of novel medicinal products or devices in healthcare and offers services in conducting complex clinical trials in a wide variety of therapeutic areas. **Overall Purpose of the...

**Overall Purpose of the Position**: Dealing primarily with study and site administration, the Clinical Trial Administrator will provide administrative support to the site and/or study team, be responsible for basic data capture, prepare and maintain source files and investigator site files according to policy, standard operating procedures and regulatory...

**Description** **Description** **Who is USP?** The U.S. Pharmacopeial Convention (USP) USP is an independent scientific organization that collaborates with the world's top experts in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that **Equity = Excellence** manifests in...

**Registered Nurse** required for clinical trial unit. Please provide registration number. Experience in clinical research with GCP qualification is preferred. Strong organizational skills and attention to detail to effectively manage multiple tasks. Excellent communication skills to interact with co-workers, patients and medical professionals. Must be...

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 complex Ability to administratively and technically/scientifically review core scientific...

Syneos Health Clinical Solutions’s job vacancy, Career and Recruitment Job title : Clinical Research Associate II jobs in Free State Job Location : Free State, Bloemfontein Deadline : April 04, 2024 Quick Recommended LinksJobs by Location Job by industries Job responsibilities Performs site qualification, site initiation, interim monitoring, site...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES 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 customer Ability to...

Are you ready to make the next step in your professional development in a global expanding company? Join Novo Nordisk as Clinic Development Centre (CDC) Project Manager and get a life-changing career This role is based in Johannesburg, South Africa and directly reports to CDC Clinical Research Manager. **The position** As CDC Project Manager, you will be...

Join us on our exciting journey IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and...

This role is primarily accountable for the end to end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. For certain studies, the Clinical Research Manager could be...

Are you ready to be a healthcare trailblazer? Do you want to spearhead the implementation of state-of-the-art digital solutions across CDC? If your answer is yes become the driving force behind local innovation, fostering efficiency and operational excellence, while building a powerful network of change partners to revolutionize trial team success. Join us...

**Minimum Qualifications & Experience** Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. Preferably experience of working in the research,...

Are you ready to make the next step in your professional development in a global expanding company? Are you interested in improving the lives of millions of people, working in a company that works with innovation and is a leader in diabetes? Join us and become a **Senior Clinical Research Associate (CRA)** in our Clinical Development Centre in South Africa...