Clinical Research Associate Job Vacancy in Ndalatando, Angola – Healthcare

Job Description

Position: Clinical Research Associate

Company: Johnson & Johnson

Location: Ndalatando, Angola

Experience: 2-4 years

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

Employment Type: Full-time

Industry: Healthcare

Department: Clinical Research

Salary: 250,000 – 400,000 SSP per month

Vacancies:1

Company Overview

Johnson & Johnson is a globally recognized leader in health care, pharmaceuticals, and medical devices, operating in more than 150 countries. In Angola, the company has a strong presence through partnerships with local distributors, hospitals, and research institutions. The organization is committed to improving health outcomes by delivering innovative products and supporting rigorous scientific research. As part of its mission to advance global health, Johnson & Johnson invests heavily in clinical development programs that address the unique health challenges faced by African populations. This commitment creates a dynamic environment for professionals seeking meaningful career opportunities in Angola.

Job Overview

The Clinical Research Associate (CRA) will play a pivotal role in managing and monitoring clinical trials conducted across Angola, ensuring compliance with regulatory standards and study protocols. Reporting to the Clinical Operations Manager, the CRA will coordinate with investigators, site staff, and internal stakeholders to facilitate high‑quality data collection and patient safety. This position offers an excellent platform for individuals passionate about advancing medical science while contributing to the local healthcare ecosystem. For more information about our commitment to career growth, visit Angola Job Search.

Key Responsibilities

• Monitor clinical trial sites in Ndalatando and surrounding regions to ensure adherence to protocol, Good Clinical Practice (GCP), and local regulations.
• Conduct site initiation, routine monitoring visits, and close‑out activities, documenting findings in detailed reports.
• Collaborate with investigators and study coordinators to resolve data discrepancies and ensure timely query resolution.
• Assist in the preparation and review of essential regulatory documents, including informed consent forms and ethics committee submissions.
• Maintain accurate source documentation and ensure proper handling of investigational products.
• Support the Clinical Operations Manager in risk assessment, site selection, and feasibility studies.
• Participate in internal training sessions and contribute to continuous improvement initiatives.

Required Skills

• Strong knowledge of GCP, ICH guidelines, and Angolan regulatory requirements.
• Excellent communication and interpersonal skills for effective collaboration with diverse stakeholders.
• Proficiency in electronic data capture (EDC) systems and Microsoft Office Suite.
• Detail‑oriented with strong organizational and time‑management abilities.
• Ability to travel frequently within Angola and adapt to varying site conditions.
• Fluency in Portuguese and working knowledge of English.

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) will be given preference.

Experience

Applicants should have 2‑4 years of hands‑on experience in clinical trial monitoring, preferably within emerging markets or African regions. Experience with multi‑site studies and familiarity with local health infrastructure are advantageous.

Salary

The compensation package ranges from 250,000 to 400,000 Angolan Kwanza (SSP) per month, commensurate with experience and qualifications. Performance‑based incentives and annual reviews are part of the remuneration structure.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Retirement savings plan aligned with Angolan labor regulations.
• Paid annual leave and statutory holidays.
• Professional development allowance for conferences and certifications.
• Transportation allowance for site visits.

Training

• On‑boarding program covering company policies, GCP, and local regulatory landscape.
• Continuous learning modules on clinical trial management systems and data analytics.
• Mentorship opportunities with senior clinical scientists.

Working Environment

The role offers a blend of office‑based work at Johnson & Johnson’s regional hub in Ndalatando and field‑based activities at clinical sites. Employees benefit from a collaborative culture that values innovation, integrity, and diversity. The company promotes a healthy work‑life balance and encourages community engagement through health 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 Johnson & Johnson careers page. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for virtual interviews.

Equal Opportunity Statement

Johnson & Johnson 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. Our hiring practices support the principles of fairness and transparency, ensuring that every applicant receives equal consideration.