Current jobs related to Snr Clinical Trial Assistant - Centurion - Novasyte
-
Clinical Trial Assistant
1 week ago
Centurion, South Africa IQVIA Full time**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,...
-
Clinical Trial Assistant 1
2 weeks ago
Centurion, Gauteng, South Africa IQVIA Full timeJob OverviewPerform 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 FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
-
Clinical Trial Assistant 1
2 weeks ago
Centurion, Gauteng, South Africa IQVIA Argentina Full timeJob OverviewPerform 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 FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
-
Clinical Trial Assistant
1 week ago
Centurion, South Africa IQVIA Full time**For GCO**: Services/deliverables include the management of all documents and logístical and administrative tasks related to trial feasibility, start-up, execution and close out of clinical trials. Ensures trial related activities are compliant with GCO SOPs, policies, code of Good Clinical Practice (GCP), Health Care Compliance requirements (HCC) and...
-
Clinical Trial Operations Coordinator
2 weeks ago
Centurion, Gauteng, South Africa IQVIA Full timeAbout the RoleWe are looking for a detail-oriented Clinical Trial Assistant to join our team at IQVIA. In this role, you will provide critical support to our clinical research teams by assisting with trial master file maintenance, document preparation, and supply coordination.Main ResponsibilitiesMaintain accurate and up-to-date records in the Trial Master...
-
Clinical Trial Coordinator
4 days ago
Centurion, Gauteng, South Africa Ampath Laboratories Full timeJob SummaryAmpath Laboratories is seeking a highly skilled Clinical Trial Coordinator to join our team. In this role, you will be responsible for coordinating the day-to-day clinical trial-related tasks within the Clinical Trials Department. Main Responsibilities:Document Management: Archive documents to ensure effective storage and retrieval of...
-
Clinical Trial Coordinator
6 days ago
Centurion, South Africa IQVIA Full time**ASSIGNMENT PROFILE** **Clinical Trial Coordinator (CTC)** **Description of Roles and Responsibilities** - **Trial and site administration**: - Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) - Ensure collation and distribution of study tools and documents - Update clinical trial databases (CTMS) and trackers - Clinical supply &...
-
Clinical Trial Logistics Coordinator
2 weeks ago
Centurion, Gauteng, South Africa Oximio Full timeJob Summary:Oximio is seeking a highly organized and detail-oriented Clinical Trial Logistics Coordinator to join our team. As a Clinical Trial Logistics Coordinator, you will be responsible for managing clinical trial logistics, including coordinating shipments, maintaining inventory levels, and ensuring compliance with regulatory standards. You will work...
-
Project Manager
4 days ago
Centurion, Gauteng, South Africa Ampath Laboratories Full timeAbout the RoleAmpath Laboratories is currently seeking a Project Manager - Clinical Trials to lead the coordination of clinical trials within our department. As a key member of our team, you will be responsible for ensuring the smooth execution of clinical trials. Key Responsibilities:Team Leadership: Lead and manage a team of staff involved in the conduct...
-
Country Clinical Trial Lead
2 weeks ago
Centurion, Gauteng, South Africa IQVIA Full timeKey ResponsibilitiesWe are seeking a highly skilled Country Clinical Trial Lead to lead local trial teams and ensure the successful execution of clinical trials. Key responsibilities include:Maintaining complete, accurate, and timely data and essential documents in systems utilized for trial management.Conducting quality local trial team meetings and...
-
Clinical Trial Coordinator
3 weeks ago
Centurion, Gauteng, South Africa IQVIA Argentina Full timeASSIGNMENT PROFILEClinical Trial Coordinator (CTC)Description of Roles and ResponsibilitiesTrial and site administration:Tracking (e.g., essential documents) and reporting (e.g., Safety Reports)Ensure collation and distribution of study tools and documentsUpdate clinical trial databases (CTMS) and trackersClinical supply & non-clinical supply management, in...
-
Clinical Trial Coordinator
3 days ago
Centurion, South Africa Labcorp Full timeLabcorp is looking to recruit a SCTA (CTC) to join our sponsor in South Africa! **Responsibilities**: **TRIAL AND SITE ADMINISTRATION**: - Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) - Ensure collation and distribution of study tools and documents o Update clinical trial databases (CTMS) and trackers - Clinical supply &...
-
Global Clinical Trials Coordinator
1 week ago
Centurion, Gauteng, South Africa IQVIA Argentina Full timeRole Summary:This position is responsible for the overall management of clinical trials in Argentina, ensuring that all studies are conducted in compliance with ICH-GCP and local regulations.Key Accountabilities:Provide operational support to central study teams and investigators.Maintain accurate and complete records of trial-related documents and...
-
Clinical Trial Product Manager
7 days ago
Centurion, Gauteng, South Africa Oximio Full timeOximio is a pharmaceutical company dedicated to delivering high-quality clinical trial products. We are seeking a Clinical Trial Product Manager to oversee the safety, quality, and compliance of these products.Responsibilities:Import Documentation: Review and approve import documentation to ensure compliance with regulatory requirements.Quality Monitoring:...
-
Trial Master File Assistant
2 weeks ago
Centurion, Gauteng, South Africa IQVIA Full timeJob DescriptionWe are seeking a highly organized and detail-focused Clinical Trial Assistant to support our clinical research teams at IQVIA. This role involves providing administrative support, maintaining accurate records, and coordinating clinical supplies.Main DutiesAssist CRAs with updating and maintaining clinical documents and systems, including the...
-
Clinical Trials Operations Manager
6 days ago
Centurion, Gauteng, South Africa IQVIA Full timeJob DescriptionThe Clinical Trials Operations Manager will be responsible for managing single and multi-service projects, ensuring quality deliverables on time and to the customer's satisfaction.Key Responsibilities:Serve as an account lead, or internal or external point of contact on standalone coding studies or accounts.Manage the customer relationship for...
-
Local Trial Manager
2 weeks ago
Centurion, Gauteng, South Africa IQVIA Full timeServices Overview: Local Trial Management services provide local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Further, services will ensure...
-
Clinical Study Support Professional
2 weeks ago
Centurion, Gauteng, South Africa IQVIA Full timeClinical Trial Assistant Role SummaryThis Clinical Trial Assistant position at IQVIA involves supporting our clinical research teams by providing administrative assistance and maintaining accurate records. You will work closely with CRAs to ensure the success of our clinical trials.
-
Clinical Trial Operations Specialist
5 days ago
Centurion, Gauteng, South Africa IQVIA Full timeJob DescriptionAbout the Role:We are seeking a skilled and experienced Clinical Trial Operations Specialist to join our team. In this role, you will be responsible for the delivery of clinical studies to meet contractual requirements.Main Responsibilities:Participate in bid defense presentations and develop integrated study management plans with the core...
-
Biostatistician
6 days ago
Centurion, South Africa FHI Clinical Inc Full time**Summary of The Position**: The Biostatistician will be responsible for biostatistical aspects, as applicable, of clinical projects undertaken by FHI Clinical, in accordance with the relevant protocol and other trial-related documentation, ICH GCP (and applicable local adaptations thereof), other local legal requirements, relevant FDA, EMA, and other...
Snr Clinical Trial Assistant
1 month ago
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 documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Collaborate with clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files and completeness.
- Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- Act as a mentor for less experienced Clinical Trial Assistants (CTAs).
- Assist with training and onboarding of new CTAs.
- May lead CTA study teams.
- May assist with interviewing and screening of potential new team members
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
- May participate in departmental quality or process improvement initiatives.
**Qualifications**:
- High School Diploma or equivalent Req
- 5 administrative support experience.
- Equivalent combination of education, training and experience.
- Minimum two years clinical research experience strongly preferred.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
- Effective written and verbal communication skills including good command of English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at