Senior Clinical Research Scientist - Oncology

Placements24; Kimberley; Hybrid; CAD 85,000 - 111,000; Full time

Benefits offered by this job

Hybrid work model

Professional growth opportunities

Conferences/Specialized training

Job summary

Our client, a globally recognized pharmaceutical company, is seeking a Senior Clinical Research Scientist to join the oncology drug development team. This hybrid role is based in Kimberley, Northern Cape, South Africa.

You will design, implement, and monitor clinical trials for novel oncology therapeutics and collaborate with investigators and regulatory agencies to advance programs. The ideal candidate holds a Ph.D.

Qualifications

• Ph.D. or MD in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
• Minimum of 6 years of experience in clinical research, with a significant focus on oncology drug development.
• Demonstrated experience in designing, executing, and managing Phase I-III clinical trials.
• Strong understanding of oncology, cancer biology, and current therapeutic approaches.
• In-depth knowledge of clinical trial methodologies, statistical principles, and regulatory requirements (e.g., FDA, EMA, SAHPRA).
• Excellent scientific acumen, analytical skills, and critical thinking abilities.
• Strong project management and organizational skills.
• Exceptional written and verbal communication skills, with the ability to effectively communicate complex scientific information.

Responsibilities

• Design and develop clinical trial protocols for oncology therapeutics.
• Oversee the operational execution of clinical trials, ensuring adherence to protocol and regulatory guidelines.
• Monitor trial progress, data quality, and patient safety.
• Collaborate with principal investigators and site staff to ensure effective trial conduct.
• Analyze clinical trial data and contribute to the interpretation of results.
• Prepare clinical study reports, regulatory submissions, and scientific publications.
• Stay current with scientific advancements in oncology and clinical trial methodologies.
• Manage relationships with external vendors and key opinion leaders in the field.
• Ensure compliance with Good Clinical Practice (GCP) and other relevant regulations.
• Provide scientific and strategic input into drug development programs.

Skills

Clinical trial design

Oncology expertise

Regulatory knowledge

Project management

Scientific communication

Education

Ph.D. or MD in Oncology/Pharmacology/Biology/Medicine

Job description

About the Role: Our client, a globally recognized pharmaceutical company at the forefront of cancer research, is seeking a Senior Clinical Research Scientist to join their oncology drug development team. This hybrid role is based in Kimberley, Northern Cape. You will play a key role in designing, implementing, and monitoring clinical trials for novel oncology therapeutics. The ideal candidate will possess a strong scientific background in oncology or a related field, extensive experience in clinical trial conduct, and a deep understanding of regulatory requirements. You will collaborate closely with internal teams, investigators, and regulatory agencies to ensure the successful progression of clinical development programs. This is a unique opportunity to contribute to the advancement of cancer treatments and make a significant impact on patient lives within South Africa, working a combination of remote and office-based days in Kimberley.

Key Responsibilities

• Design and develop clinical trial protocols for oncology therapeutics.
• Oversee the operational execution of clinical trials, ensuring adherence to protocol and regulatory guidelines.
• Monitor trial progress, data quality, and patient safety.
• Collaborate with principal investigators and site staff to ensure effective trial conduct.
• Analyze clinical trial data and contribute to the interpretation of results.
• Prepare clinical study reports, regulatory submissions, and scientific publications.
• Stay current with scientific advancements in oncology and clinical trial methodologies.
• Manage relationships with external vendors and key opinion leaders in the field.
• Ensure compliance with Good Clinical Practice (GCP) and other relevant regulations.
• Provide scientific and strategic input into drug development programs.

Requirements

• Ph.D. or MD in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
• Minimum of 6 years of experience in clinical research, with a significant focus on oncology drug development.
• Demonstrated experience in designing, executing, and managing Phase I-III clinical trials.
• Strong understanding of oncology, cancer biology, and current therapeutic approaches.
• In-depth knowledge of clinical trial methodologies, statistical principles, and regulatory requirements (e.g., FDA, EMA, SAHPRA).
• Excellent scientific acumen, analytical skills, and critical thinking abilities.
• Strong project management and organizational skills.
• Exceptional written and verbal communication skills, with the ability to effectively communicate complex scientific information.
• Ability to work collaboratively in a cross-functional team environment.
• Experience with data analysis and interpretation for clinical trials is essential for this hybrid role in Kimberley.

Benefits

• Competitive salary, comprehensive health and wellness benefits, and a generous performance bonus program.
• Employees are provided with opportunities for professional growth, including attendance at international conferences and specialized training.
• Join a dedicated team committed to improving patient outcomes in oncology in Kimberley.
• We offer a dynamic and collaborative work environment with a flexible hybrid work model.
• This position is based at our research and development hub in the Northern Cape province, South Africa.