Medical Researcher Deputy Director (Specialist Medical Doctor)_Jhb

Pro Tem; Johannesburg; On-site; ZAR 1,200,000 - 1,800,000; Full time

Job summary

A leading company in medical research seeks a Medical Researcher Deputy Director to oversee clinical trials and drive innovation. The successful candidate will possess an MBChB and have extensive experience in clinical research, ensuring regulatory compliance and guiding research strategy aligned with the organization’s goals. This office-based position may require travel and flexibility outside regular hours.

Qualifications

• MBChB / Medical Doctor qualifications required.
• Experience in clinical research and pharmaceutical industry preferred.
• Prior experience using AI in research is a strong advantage.

Responsibilities

• Lead design and execution of Phase I–IV clinical trials.
• Ensure adherence to regulatory compliance and GCP standards.
• Analyze and interpret clinical data for decision-making.

Skills

Strategic thinking

Leadership

Collaboration

High ethical standards

Education

MBChB / Medical Doctor with Specialty Qualifications

Job description

Medical Researcher Deputy Director (Specialist Medical Doctor)

Business Unit : Medical Research Department

Location: Parktown, Johannesburg

Reports to: [Specify supervisor if available]

Number of Immediate Subordinates / Direct Reports: 1

Main Purpose of Job

To lead the design, execution, and oversight of all clinical research and development programs within the company. The Medical Research Deputy Director will apply medical and scientific expertise to drive innovation, oversee clinical trial design and execution, ensure regulatory compliance, and support the development of safe and effective pharmaceutical products aligned with the organization’s strategic objectives.

To oversee the Medical Affairs in the company.

Key Performance Areas

Clinical Trial Leadership

• Lead the design and execution of Phase I–IV clinical trials, ensuring scientific and ethical integrity.
• Review and approve study protocols, investigator brochures, and clinical development plans.

Medical Oversight

• Provide clinical guidance on drug development projects.
• Serve as the medical expert in cross-functional project teams.

Regulatory Compliance

• Ensure adherence to GCP (Good Clinical Practice), ICH guidelines, and SAHPRA regulations.
• Support the preparation of clinical sections of regulatory submissions and responses to authorities.

Scientific Innovation

• Guide research strategy and medical innovation aligned with therapeutic focus areas.
• Evaluate opportunities for new molecules, reformulations, and indications.
• Collaborate with researchers, medical writers, and clinical operations staff.
• Foster a high-performance, learning-oriented environment.

Stakeholder Engagement

• Liaise with Key Opinion Leaders (KOLs), investigators, and academic institutions.
• Represent the company at scientific conferences and advisory boards.

Data Review & Interpretation

• Analyze and interpret clinical data for decision-making, ensuring data integrity, safety reporting, and ethical standards.

Cross-Functional Collaboration & Integration

Work closely with Regulatory Affairs, Pharmacovigilance, Medical Affairs, and Marketing to align research with commercial and regulatory goals.

Qualifications

• MBChB / Medical Doctor with Specialty Qualifications.

Experience

• Experience in clinical research and execution of clinical trials.
• Experience in the pharmaceutical industry is an advantage.

Additional Advantage

• Prior experience using AI in research is highly advantageous.

Skills / Competencies

• Strategic thinking and high attention to detail.
• Leadership, collaboration, and cross-functional communication skills.
• High ethical standards and commitment to patient safety.

Working Conditions

• Office-based with business travel as required.
• Flexibility to work outside regular hours as needed.