Clinical Trials Manager - Pharmaceutical Sector

Placements24; Kempton Park; Hybrid; ZAR 900,000 - 1,300,000; Full time

Benefits offered by this job

Health insurance

Retirement savings plan

Performance-based bonus

Professional development opportunities

Job summary

Placements24 is seeking a Clinical Trials Manager in Gauteng to oversee planning, execution, and completion of Phase I–IV trials. The role requires strong project leadership and a deep understanding of regulatory requirements to drive compliant, efficient research programs.

The successful candidate will manage sites, vendors, data, and multidisciplinary teams across locations, ensuring timelines, budgets, and quality meet corporate standards and patient safety remains paramount.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related; Master's preferred.
• Minimum 5 years' experience in clinical trial management in pharma/biotech.
• Experience in all phases of clinical trials (Phase I–IV).
• Knowledge of GCP, ICH guidelines, and regulatory submission processes.
• Strong project management and ability to manage multiple complex projects.
• Excellent leadership, communication, and interpersonal skills.
• Experience in data management and statistical analysis interpretation.
• Willingness to travel to investigative sites and meetings.
• Ability to work effectively in a remote setting, managing teams across locations.
• Familiarity with regulatory environment in Tembisa, Gauteng is a plus.

Responsibilities

• Develop and manage clinical trial protocols, budgets, and timelines.
• Oversee selection, training, and management of clinical investigative sites and site staff.
• Ensure adherence to Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable local and international regulatory requirements.
• Monitor clinical trial progress, identify potential risks, and implement mitigation strategies.
• Manage data collection, review, and database lock processes.
• Coordinate with internal departments, including regulatory affairs, medical affairs, and pharmacovigilance.
• Prepare and present trial status reports to senior management and key stakeholders.
• Manage vendor relationships and ensure successful execution of outsourced activities.
• Facilitate site audits and regulatory inspections.
• Contribute to the development and improvement of clinical trial operational procedures.

Skills

Clinical trial management

Leadership

Communication

Interpersonal skills

Project management

Remote team management

Regulatory knowledge

Education

Bachelor's degree in Life Sciences/Nursing/Pharmacy

Master's degree or higher (preferred)

Job description

About the Role

Our client, a distinguished name in the pharmaceutical landscape, is actively seeking a highly skilled and dedicated Clinical Trials Manager to oversee critical research initiatives. This impactful position is located in Tembisa, Gauteng . The Clinical Trials Manager will be instrumental in the planning, execution, and completion of Phase I-IV clinical trials, ensuring compliance with all relevant regulatory standards and company policies. This is a vital role within our organization, focused on bringing innovative pharmaceutical products to market efficiently and ethically. The successful candidate will possess exceptional project management skills and a deep understanding of clinical trial operations within the pharmaceutical industry. They will be a key player in driving our research forward and contributing to significant advancements in healthcare. This role requires a proactive approach and a commitment to excellence in all aspects of clinical trial management.

Key Responsibilities

• Develop and manage comprehensive clinical trial protocols, budgets, and timelines.
• Oversee the selection, training, and management of clinical investigative sites and site staff.
• Ensure adherence to Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable local and international regulatory requirements.
• Monitor clinical trial progress, identify potential risks, and implement mitigation strategies.
• Manage data collection, review, and database lock processes.
• Coordinate with internal departments, including regulatory affairs, medical affairs, and pharmacovigilance.
• Prepare and present trial status reports to senior management and key stakeholders.
• Manage vendor relationships and ensure successful execution of outsourced activities.
• Facilitate site audits and regulatory inspections.
• Contribute to the development and improvement of clinical trial operational procedures.

Requirements

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline; Master's degree or higher is preferred.
• Minimum of 5 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
• Proven experience in managing all phases of clinical trials (Phase I-IV).
• In-depth knowledge of GCP, ICH guidelines, and regulatory submission processes.
• Strong project management skills with the ability to manage multiple complex projects simultaneously.
• Excellent leadership, communication, and interpersonal skills.
• Experience in data management and statistical analysis interpretation.
• Ability to travel as required to investigative sites and relevant meetings.
• Demonstrated ability to work effectively in a remote setting, managing teams and projects across different locations.
• Familiarity with the pharmaceutical research environment in Tembisa, Gauteng is a plus.

Benefits

Our client offers a competitive salary package, comprehensive health insurance, retirement savings plan, and performance-based bonuses. We provide extensive opportunities for professional growth and development, including access to training programs and conferences. This role comes with a significant degree of autonomy and the chance to make a tangible impact on patient lives through groundbreaking pharmaceutical research. Join a forward-thinking organization that prioritizes innovation, collaboration, and employee well-being. Enjoy a dynamic and supportive work culture with excellent work-life balance provisions.