Job Description
Position: Clinical Research Associate
Company: Merck Angola
Location: Luanda, Angola
Experience: 3-5 years in clinical research or pharmaceutical development
Education: Bachelor’s Degree in Life Sciences, Pharmacy, or related field
Employment Type: Full-Time
Industry: Pharmaceutical Research and Development
Department: Clinical Trials and Drug Development
Salary: 1,500,000 – 2,500,000 SSP
Vacancies:1
Company Overview
Merck Angola, a subsidiary of Merck & Co., Inc., is a global leader in pharmaceutical innovation and healthcare solutions. With a commitment to advancing medical research and improving patient outcomes, Merck Angola plays a pivotal role in developing cutting-edge therapies tailored to the unique health challenges of the region. The company fosters a collaborative environment where professionals can contribute to groundbreaking research while adhering to the highest standards of ethical practice.
Job Overview
Merck Angola is seeking a dedicated Clinical Research Associate to join its dynamic team in Luanda. This role involves overseeing clinical trials, ensuring compliance with regulatory standards, and contributing to the development of life-saving pharmaceutical products. Candidates will have the opportunity to work on innovative projects that align with Angola’s healthcare priorities while gaining exposure to international research protocols. For more Angola Jobs, visit our platform.
Key Responsibilities
- Monitor and manage clinical trials to ensure adherence to Good Clinical Practice (GCP) guidelines.
- Coordinate with healthcare professionals, researchers, and regulatory bodies to facilitate trial execution.
- Review and analyze trial data for accuracy, completeness, and compliance.
- Prepare detailed reports and documentation for internal and external audits.
- Identify and resolve site-specific issues to maintain trial timelines and quality standards.
Required Skills
- Proven experience in clinical research, preferably within pharmaceutical or biotechnology sectors.
- Strong understanding of regulatory frameworks (e.g., ICH, FDA, EMA).
- Excellent analytical and problem-solving abilities.
- Proficiency in data management tools and clinical trial software.
- Fluency in Portuguese and English; additional regional languages are an asset.
Education
Candidates must hold a Bachelor’s Degree in Life Sciences, Pharmacy, or a related discipline. Advanced certifications such as CCRA (Certified Clinical Research Associate) are highly advantageous.
Experience
Applicants should have a minimum of 3–5 years of hands-on experience in clinical research, with a focus on trial monitoring, data validation, and regulatory compliance. Experience in both Phase I–IV trials is preferred.
Salary
This position offers a competitive salary range of 1,500,000 to 2,500,000 Angolan Kwanza (SSP), commensurate with experience and qualifications.
Benefits
- Comprehensive health insurance coverage for employees and dependents.
- Performance-based bonuses and annual salary reviews.
- Professional development opportunities, including access to global training programs.
- Flexible work arrangements and remote collaboration tools.
- Relocation assistance for qualified candidates.
Training
- Onboarding training to familiarize with Merck’s internal systems and protocols.
- Workshops on advanced clinical trial management and regulatory updates.
- Leadership development programs for career progression.
Working Environment
Merck Angola promotes a culture of innovation, integrity, and inclusivity. The workplace is equipped with modern facilities, including state-of-the-art laboratories and collaborative workspaces. The role requires occasional travel to trial sites across Angola and regional partnerships.
Application Process
To apply, submit your CV and a cover letter to the official Merck Angola careers portal. Shortlisted candidates will be contacted for interviews and practical assessments. For more Career Opportunities in Angola, explore our partner platforms.
Equal Opportunity Statement
Merck Angola is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Decisions are based on merit, qualifications, and business needs.