Cra 2
2 weeks ago
Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
- Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support project/site start-up phase.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Act as a mentor for new clinical staff including conducting co-monitoring and training visits.
- May provide assistance with design of study tools, documents and processes.
- Convey features and opportunities of study to site.
- Collaborate and liaise with study team members for project execution support as appropriate.
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Snr Cra 2
1 week ago
Centurion, South Africa IQVIA Full timeWhether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone - you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.Award...
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Associate Cra
1 week ago
Centurion, South Africa IQVIA Full timeJob Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. - Essential Functions - Complete appropriate therapeutic, protocol and clinical research...
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Local Study Lead
7 months ago
Centurion, South Africa Novasyte Full timeTypical Accountabilities - Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. - Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies - Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with sponsor...
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Centralized Trip Report Reviewer
3 days ago
Centurion, South Africa Labcorp Full timeHere at Labcorp Drug Development we are currently recruiting for a Centralized Trip Report Reviewer in South Africa. Responsibilities will include: - Management of projects under direction of a Project Manager / Director as assigned. - Ensure site monitoring responsibility for clinical studies are conducted according to Covance Standard Operating...
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Clinical Trial Coordinator
2 weeks 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 &...
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Associate Laboratory Project Services Manager
2 weeks ago
Centurion, South Africa Q² Solutions Full timeJob Overview Under general direction, manage all laboratory aspects of assigned clinical trial projects for a Customer or a specific program for a Customer. May have responsibility for a specific Customer, drug program, indication or drug compound. Acts as the main point of contact for the Customer after study award and throughout the entire study lifecycle...
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Assoc Lab Project Services Mgr
2 weeks ago
Centurion, South Africa IQVIA Full timeJob Overview Under general direction, manage all laboratory aspects of assigned clinical trial projects for a customer or a specific program for a customer. May have responsibility for a specific Customer, drug program, indication or drug compound. Acts as the main point of contact for the Customer after study award and throughout the entire study lifecycle...
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Project Manager
7 months ago
Centurion, South Africa Q² Solutions Full timeJob Overview Under general direction, manage all laboratory aspects of assigned clinical trial projects for a Customer or a specific program for a Customer. May have responsibility for a specific Customer, drug program, indication or drug compound. Acts as the main point of contact for the Customer after study award and throughout the entire study lifecycle...
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Laboratory Project Services Manager
7 months ago
Centurion, South Africa Novasyte Full timeJob Overview Under general direction, manage all laboratory aspects of assigned clinical trial projects for a Customer or a specific program for a Customer. May have responsibility for a specific Customer, drug program, indication or drug compound. Acts as the main point of contact for the Customer after study award and throughout the entire study lifecycle...