Associate Clinical Research Associate (CRA) – Nairobi, Kenya

Associate Clinical Research Associate (CRA) – Nairobi, Kenya

Location: Nairobi, Kenya
Job Type: Full-Time
Reference Number: R1444049
Available in Additional Locations
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Job Overview

IQVIA is seeking a passionate and motivated Associate Clinical Research Associate (CRA) to join our global team in Nairobi, Kenya. This position offers the opportunity to gain hands-on experience in clinical research, working closely with experienced professionals. You will engage in a structured training program that equips you with the knowledge and skills required to independently conduct clinical monitoring visits. This role ensures adherence to study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements, contributing to the advancement of innovative medical treatments that improve patient outcomes.

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Key Responsibilities

As an Associate CRA, you will have the opportunity to develop and enhance your skills in various aspects of clinical research. Your primary responsibilities include:

1. Structured Training and Development

• Engage in comprehensive therapeutic, protocol, and clinical research training to acquire the skills necessary for independent clinical monitoring.
• Gain practical experience by collaborating with experienced clinical staff on study procedures and clinical trial protocols.

2. Clinical Monitoring Visits

• Under close supervision, conduct site monitoring visits, including site selection, initiation, monitoring, and close-out visits, to ensure compliance with study protocols and Good Clinical Practices (GCP).
• Administer protocol-related training to assigned clinical sites, establishing clear lines of communication and managing project expectations.

3. Quality Control and Compliance

• Evaluate the quality and integrity of study site practices to ensure adherence to the protocol and regulatory requirements. Escalate quality issues as appropriate.
• Ensure that site documents are properly maintained in compliance with Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.

4. Study Management and Tracking

• Assist in managing the progress of clinical studies by tracking regulatory submissions, patient recruitment, enrollment rates, and Case Report Form (CRF) completion.
• Generate and resolve data queries and ensure timely submission of study documentation to the Trial Master File (TMF).

5. Documentation and Reporting

• Maintain appropriate documentation, including monitoring visit findings, action plans, and follow-up letters. Submit regular visit reports and other study-related documentation to ensure transparency and compliance.

6. Collaboration and Teamwork

• Collaborate with study team members to support project execution and site management.
• Contribute to the development of subject recruitment plans and track recruitment progress at clinical sites.

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Qualifications and Skills

To excel in this role, you should possess the following qualifications and skills:

Educational Background

• Bachelor’s degree in a scientific discipline or healthcare preferred. An equivalent combination of education, training, and experience may be considered.
• Prior clinical research experience is preferred but not required.

Technical Skills

• Proficient in Microsoft Word, Excel, PowerPoint, and other relevant software applications.
• Experience using laptops, iPhones, and iPads is a plus.

Communication and Problem-Solving

• Strong written and verbal communication skills with proficiency in English.
• Excellent organizational and problem-solving skills to manage clinical research processes effectively.

Regulatory Knowledge

• Knowledge of Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and other clinical research regulatory requirements.

Interpersonal Skills

• Ability to build and maintain effective working relationships with colleagues, managers, and clients.
• Demonstrated time management and financial management skills.

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Why Join IQVIA?

IQVIA is a global leader in clinical research and healthcare solutions, dedicated to improving patient outcomes and population health. Joining IQVIA means:

• Being part of a global team that collaborates to deliver innovative solutions in clinical research.
• Access to a comprehensive training program that equips you with the necessary skills for career advancement in clinical research.
• Working on impactful projects that contribute to the development of new medical treatments.

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Company Overview

IQVIA is a world-leading provider of clinical research services, healthcare intelligence, and commercial insights. We help healthcare organizations make better decisions, accelerating medical innovation. Our expertise in clinical research, data analytics, and patient outcomes puts us at the forefront of life sciences advancements.

For more information, visit our website: https://jobs.iqvia.com

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Call to Action: Apply Now!

Are you ready to take the next step in your clinical research career? Apply now to join IQVIA and become a vital part of a team committed to improving healthcare outcomes worldwide.

Apply Now

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Application Process

To apply for this position:

1. Click the Apply Now button.
2. Submit your updated resume.
3. Complete the application form with your contact information and job history.

For any questions or concerns, please contact our recruitment team at: recruitment@iqvia.com.

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Job Summary

This role as an Associate CRA is designed for individuals passionate about clinical research and dedicated to improving patient outcomes through the development of innovative medical treatments. You will work closely with experienced clinical research professionals and engage in a structured training program that will equip you with essential skills for career growth.

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TELEGRAM CHANNEL

Join IQVIA and embark on a fulfilling career in clinical research. As an Associate CRA, you will play a critical role in advancing healthcare solutions while gaining valuable experience through hands-on training. Our mission is to create intelligent connections that accelerate the development and commercialization of innovative medical treatments worldwide.

Share this Opportunity: Feel free to share this job with friends, colleagues, and professionals who may be interested. Sharing this opportunity will help us connect with passionate individuals eager to make a difference in the world of clinical research.

We look forward to welcoming you to our team at IQVIA.