Senior Clinical Research Associate Job Vacancy in Nimule, South Sudan – Pharmaceuticals & Biotechnology

Job Description

Position: Senior Clinical Research Associate

Company: GlaxoSmithKline

Location: Nimule, South Sudan

Experience: 5+ years in clinical research

Education: Bachelor’s degree in Life Sciences or related field; Master’s preferred

Employment Type: Full-time

Industry: Pharmaceuticals & Biotechnology

Department: Clinical Research

Salary: SSP 30,000,000 – SSP 45,000,000 per annum

Vacancies:1

Company Overview

GlaxoSmithKline (GSK) is a global healthcare leader dedicated to improving the quality of life through innovative medicines, vaccines, and consumer health products. With a presence in over 150 countries, GSK combines scientific expertise with a deep commitment to community health. In South Sudan, GSK supports local health initiatives, collaborates with ministries, and works to strengthen the pharmaceutical supply chain. The company’s mission aligns with the broader goal of advancing health outcomes across the region, making it an attractive employer for professionals seeking to make a tangible impact. As part of its expansion strategy, GSK is establishing a robust clinical research hub in Nimule, a strategic border town that offers unique opportunities for cross‑border health studies and community engagement. This role contributes directly to GSK’s vision of delivering breakthrough therapies to patients in South Sudan and beyond, reinforcing the company’s reputation as a trusted partner in the global health ecosystem.

Job Overview

The Senior Clinical Research Associate will lead and oversee clinical trial activities for GSK’s pharmaceutical pipeline in South Sudan. Reporting to the Clinical Operations Manager, you will be responsible for ensuring that studies are conducted in compliance with international Good Clinical Practice (GCP) standards, local regulatory requirements, and GSK’s internal policies. This position involves close collaboration with investigators, site staff, and external partners to drive high‑quality data collection and patient safety. You will also serve as a key liaison between GSK’s global research teams and local sites, facilitating seamless communication and knowledge transfer. For more information about GSK’s commitment to career growth, visit South Sudan Job Search. This role offers a unique platform to contribute to life‑changing medical research while developing a deep understanding of the South Sudanese healthcare landscape.

Key Responsibilities

• Plan, initiate, and monitor clinical trial sites in Nimule and surrounding regions.
• Ensure adherence to GCP, local regulations, and GSK SOPs throughout study conduct.
• Conduct site initiation visits, routine monitoring, and close‑out activities.
• Manage source data verification, query resolution, and documentation of trial findings.
• Collaborate with investigators to ensure patient recruitment targets are met ethically and efficiently.
• Prepare and review regulatory submissions, safety reports, and study progress updates.
• Train site staff on protocol specifics, data capture tools, and adverse event reporting.
• Maintain accurate trial master files and ensure timely communication with global project teams.

Required Skills

• Strong knowledge of GCP, ICH guidelines, and local regulatory frameworks.
• Excellent analytical and problem‑solving abilities.
• Effective communication and interpersonal skills for stakeholder engagement.
• Proficiency in electronic data capture (EDC) systems and Microsoft Office Suite.
• Ability to travel within South Sudan and neighboring regions as required.
• Detail‑oriented mindset with a commitment to data integrity.

Education

A minimum of a Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related discipline is required. Candidates holding a Master’s degree or relevant certifications (e.g., Certified Clinical Research Professional) are highly preferred and will be considered favorably during the selection process.

Experience

Applicants must possess at least five years of hands‑on experience in clinical research monitoring or site management, preferably within the pharmaceutical or biotechnology sectors. Experience conducting trials in low‑resource settings or emerging markets is an advantage, as is familiarity with South Sudan’s health infrastructure.

Salary

The compensation package ranges from SSP 30,000,000 to SSP 45,000,000 per annum, commensurate with experience, qualifications, and performance. Salary is paid monthly and includes statutory benefits as per South Sudan labor law.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Annual leave and sick leave in line with local regulations.
• Performance‑based bonuses and incentives.
• Professional development allowance for conferences and certifications.
• Relocation assistance for candidates moving to Nimule.

Training

• On‑boarding program covering GSK’s corporate culture, compliance, and systems.
• Continuous GCP and regulatory training modules.
• Mentorship from senior global clinical research leaders.
• Access to GSK’s internal learning platform for skill enhancement.

Working Environment

GSK offers a collaborative, inclusive, and safety‑focused workplace. The Nimule office is equipped with modern facilities, reliable internet connectivity, and a supportive team environment. Employees benefit from flexible working arrangements where feasible, and the organization promotes a healthy work‑life balance through wellness initiatives and community outreach programs.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online portal on the South Sudan Job Search website. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for virtual interviews followed by an on‑site assessment in Nimule.

Equal Opportunity Statement

GlaxoSmithKline is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, race, religion, age, disability, or sexual orientation. All qualified applicants will receive consideration for employment without regard to any protected characteristic.