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About the Organisation
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide
Clinical Research Associate job at IQVIA | Apply Now
Uganda
IQVIA, established in 1982 by Dennis Gillings, is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Formed through the 2016 merger of Quintiles and IMS Health, the company operates in over 100 countries with a workforce of approximately 88,000 employees. Recognized as one of the world's largest contract research organizations, IQVIA offers services that span the entire healthcare continuum, including clinical development, commercialization, and data analytics.
The organization fosters a work culture centered on core values such as integrity, transparency, and accountability, providing employees with opportunities to engage in innovative projects that drive meaningful change in global healthcare. IQVIA's business model emphasizes leveraging big data and transformative technology to deliver actionable insights, partnering with clients to accelerate the development and delivery of medical treatments. The company is also committed to corporate social responsibility, engaging in initiatives aimed at improving healthcare outcomes worldwide. For more information, visit their website at www.iqvia.com.
Are you looking for Healthcare/ Medicine jobs in Uganda 2024 today? then you might be interested in Clinical Research Associate job at IQVIA
Full Time
Deadline:
20 Dec 2024
Job Title
Clinical Research Associate job at IQVIA
IQVIA
Job Description
Uganda
Full time
R1445343
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Duties, Roles and Responsibilities
Qualifications, Education and Competencies
See all details of the qualifications, competencies and education for this role under the "How to Apply" section below.
APPLICATIONS FOR THIS POSITION MUST BE ONLINE
Click the "Apply Button" Below to submit your Application
Deadline: 20th December 2024
Find application details and links on the AfriCareers Jobs Portal:
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Click the Apply button below
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Go to the "Jobs" tab
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Read the detailed job description, Roles and Qualifications.
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Submit your application via the jobs portal
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Track progress under "My Applications" tab
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How to Apply
Essential Functions
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
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 start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
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.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
SERVICES
COMMERCIAL
SERVICES
INDUSTRIAL
SERVICES
RESIDENTIAL
Qualifications
Bachelor's Degree Degree in scientific discipline or health care preferred. Req
Requires at least 1 year of on-site monitoring experience. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree. Req
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
