Clinical Research Manager

Placements24; Sandton; On-site; ZAR 900,000 - 1,800,000; Full time

Benefits offered by this job

Competitive salary

Executive medical & dental insurance

Retirement plan

Job summary

Placements24 is seeking an experienced Clinical Research Manager in Sandton to oversee and direct complex clinical trial operations, from protocol development to final reporting. You will manage a team of clinical research professionals, ensuring timeliness, budget adherence, and regulatory compliance.

The ideal candidate will have strong project management skills, deep understanding of trial phases, and a proven ability to lead teams effectively in a leading pharmaceutical setting.

Qualifications

• Oversee budgets, timelines, and resources for clinical trials.
• Lead and develop a team of CRAs and staff.
• Ensure all activities comply with ICH-GCP and regulatory standards.

Responsibilities

• Develop and manage trial budgets, timelines, and resources.
• Oversee the planning, execution, and monitoring of multiple trials.
• Lead, mentor, and develop CRAs and clinical staff.
• Ensure compliance with ICH-GCP, regulations, and SOPs.

Skills

Leadership

Clinical Research

Project Management

GCP

Education

Bachelor's degree in life sciences

Master's degree preferred

Tools

CTMS

EDC

Job description

About the Role

Our client is seeking an experienced and dynamic Clinical Research Manager to oversee and direct their clinical trial operations in Sandton, Gauteng . This leadership role is essential for ensuring the successful execution of clinical studies, from protocol development through to final reporting. You will manage a team of clinical research professionals, ensuring adherence to timelines, budgets, and regulatory standards, including Good Clinical Practice (GCP). The ideal candidate possesses strong project management skills, a comprehensive understanding of clinical trial phases, and a proven ability to lead teams effectively. This position requires a strategic thinker with excellent communication and problem-solving capabilities, dedicated to advancing medical treatments through rigorous clinical research. You will be instrumental in fostering a high-performance culture within the clinical research department, ensuring the integrity and quality of all study-related activities. This is a significant opportunity to drive impactful research outcomes within a leading pharmaceutical organization. We are committed to supporting our management team with the resources and autonomy needed to achieve excellence in clinical research endeavors, contributing significantly to patient well-being.

Key Responsibilities

• Develop and manage clinical trial budgets, timelines, and resources.
• Oversee the planning, execution, and monitoring of multiple clinical trials simultaneously.
• Lead, mentor, and develop a team of Clinical Research Associates (CRAs) and other clinical staff.
• Ensure all clinical trial activities comply with ICH-GCP, local regulations, and company SOPs.
• Select, train, and manage clinical investigators and site staff.
• Oversee the collection, quality, and analysis of clinical trial data.
• Liaise with regulatory authorities, ethics committees, and other external stakeholders.
• Manage vendor relationships (e.g., CROs, central labs) as applicable.
• Prepare and review clinical study reports (CSRs) and other regulatory submission documents.
• Contribute to the development of clinical trial protocols and study designs.

Requirements

• Bachelor's degree in a life science, healthcare field, or equivalent.
• Master's degree or higher preferred.
• Minimum of 7 years of progressive experience in clinical research, with at least 3 years in a management or supervisory role.
• Extensive experience managing Phase I, II, III, or IV clinical trials across various therapeutic areas.
• In-depth knowledge of clinical trial methodology, regulatory requirements, and GCP.
• Proven leadership and team management skills, with the ability to motivate and develop staff.
• Strong project management capabilities, including budget and timeline management.
• Excellent communication, negotiation, and interpersonal skills.
• Proficiency in clinical trial management systems (CTMS), Electronic Data Capture (EDC) systems, and relevant software.
• Ability to travel as required for site visits, meetings, and training.
• Strategic thinking and strong problem-solving abilities.

Benefits

• Highly competitive salary and annual performance bonus structure.
• Comprehensive executive medical, dental, and vision insurance plans.
• Generous retirement savings plan with company contributions.
• Substantial annual leave and paid time off benefits.
• Opportunities for advanced leadership training and professional development.
• Access to cutting-edge clinical research technologies and methodologies.
• A dynamic and collaborative leadership environment.
• Company-provided vehicle or generous car allowance.
• Employee assistance program and wellness initiatives.
• Significant impact on advancing medical research and patient care.