Clinical Research Operations Director Job Vacancy in Tamarin, Mauritius – Pharmaceutical Research & Clinical Trials

Job Description

Position:Clinical Research Operations Director

Company:IQVIA Mauritius Ltd

Location:Tamarin, Mauritius

Experience:Minimum 10 years in clinical research operations with at least 5 years in senior leadership roles

Education:Master’s degree in Life Sciences, Medicine, Pharmacy, or related field; PhD preferred

Employment Type:Full-time

Industry:Pharmaceutical Research & Clinical Trials

Department:Clinical Operations

Vacancies:1

Company Overview

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With operations in more than 100 countries, IQVIA delivers innovative solutions that drive healthcare forward. Our Mauritius office serves as a strategic hub for clinical research operations across Africa and the Indian Ocean region, leveraging the country’s excellent infrastructure, multilingual talent pool, and favorable regulatory environment. We are committed to advancing clinical research through scientific rigor, operational excellence, and technological innovation. As we expand our presence in Mauritius, we seek visionary leaders who can drive our clinical research initiatives while contributing to the growth of the life sciences sector in the region.

Job Overview

We are seeking an experienced Clinical Research Operations Director to lead our clinical trial operations in Mauritius and oversee regional clinical research activities. This senior leadership position requires strategic vision, operational expertise, and the ability to manage complex clinical research programs across multiple therapeutic areas. The successful candidate will be responsible for ensuring the successful execution of clinical trials while maintaining the highest standards of quality, compliance, and patient safety. This role offers an exceptional opportunity to shape the future of clinical research in Mauritius while working with global pharmaceutical and biotechnology companies. For more Mauritius Jobs and career opportunities, visit our comprehensive job portal at https://mauritiusjobsearch.com.

Key Responsibilities

• Develop and implement strategic plans for clinical research operations in Mauritius and the surrounding region
• Oversee the management of multiple clinical trials across various therapeutic areas including oncology, infectious diseases, and chronic conditions
• Ensure compliance with international regulatory requirements (ICH-GCP), local regulations, and company SOPs
• Manage clinical operations budgets, resource allocation, and timeline adherence for all assigned projects
• Lead and mentor a team of clinical research professionals including clinical research managers, monitors, and coordinators
• Establish and maintain strong relationships with investigative sites, key opinion leaders, and regulatory authorities
• Implement quality management systems and risk mitigation strategies for clinical trial operations
• Drive process improvements and innovation in clinical trial execution through technology adoption and best practices
• Represent IQVIA at industry conferences, regulatory meetings, and business development activities
• Ensure patient safety and data integrity throughout the clinical trial lifecycle

Required Skills

• Expert knowledge of ICH-GCP guidelines and global clinical research regulations
• Proven leadership abilities with experience managing large, multidisciplinary teams
• Excellent strategic planning and business acumen in clinical research operations
• Strong financial management skills including budgeting and resource allocation
• Exceptional communication and stakeholder management capabilities
• Advanced problem-solving and decision-making skills in complex clinical scenarios
• Proficiency in clinical trial management systems and electronic data capture platforms
• Ability to navigate multicultural environments and manage diverse teams
• Strong negotiation and conflict resolution skills
• Commitment to quality, ethics, and patient safety in clinical research

Education

Candidates must possess a Master’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or a related scientific discipline. A PhD or MD degree is highly preferred. Additional certifications in clinical research (CCRP, CCRC) or project management (PMP) are advantageous. Continuous professional development in clinical research methodology, regulatory affairs, or leadership is expected.

Experience

A minimum of 10 years of progressive experience in clinical research operations is required, with at least 5 years in senior leadership positions managing clinical trial portfolios. Candidates must demonstrate experience overseeing Phase I-IV clinical trials across multiple therapeutic areas. International experience managing clinical operations in emerging markets is essential. Proven track record of successful regulatory inspections and audit outcomes is required. Experience in business development, proposal writing, and client relationship management is preferred.

Benefits

• Competitive executive compensation package with performance-based incentives
• Comprehensive health insurance including dental and vision coverage
• Retirement savings plan with company matching contributions
• Professional development budget for conferences and advanced training
• Flexible working arrangements with remote work options
• Generous annual leave and public holiday entitlements
• Relocation assistance for international candidates
• Company vehicle or transportation allowance
• Wellness program including gym membership and health screenings
• Opportunities for international travel and global career advancement

Training

• Comprehensive onboarding program including company systems and processes
• Advanced leadership development program for senior executives
• Regular training on evolving regulatory requirements and industry standards
• Technology training on clinical trial management systems and analytics platforms
• Cross-cultural management and global team leadership workshops
• Mentorship program with senior IQVIA leaders worldwide
• Continuous professional education in clinical research methodology
• Quality management and audit preparedness training
• Business development and client management skill development
• Innovation and digital transformation in clinical research workshops

Working Environment

This position is based in our modern Tamarin office with state-of-the-art facilities designed to support clinical research operations. The role involves a combination of office-based work, site visits, and international travel (approximately 30%). We foster a collaborative, innovative, and ethical work culture where scientific excellence and patient safety are paramount. The Clinical Research Operations Director will work with a diverse team of professionals from various cultural and scientific backgrounds, contributing to IQVIA’s mission of advancing human health through data science and clinical research.

Application Process

Interested candidates should submit a comprehensive CV, cover letter detailing their clinical research leadership experience, and contact information for three professional references through our online application portal. The selection process includes initial screening, competency-based interviews, case study presentation, and final executive interview. Only shortlisted candidates will be contacted for interviews. The application deadline is 30 days from the posting date. For additional Job Vacancy in Mauritius opportunities across various sectors, explore https://www.southafricajobsearch.com/.

Equal Opportunity Statement

IQVIA is an equal opportunity employer committed to creating a diverse and inclusive workplace. We welcome applications from all qualified individuals regardless of race, ethnicity, religion, gender, sexual orientation, age, disability, or any other protected characteristic. We believe that diversity drives innovation and excellence in clinical research. Our commitment to equal opportunity extends to all aspects of employment including recruitment, hiring, promotion, compensation, and professional development. We are dedicated to providing reasonable accommodations for candidates with disabilities throughout the recruitment process.