Senior Clinical Research Scientist

Placements24; Polokwane; Hybride; ZAR 1 200 000 - 1 800 000; Plein temps

Avantages offerts par ce poste

Competitive salary and annual bonus.

Comprehensive health, dental, and eye/

Generous paid time off and holidays.

Retirement savings plan with company-m

Professional development opportunities

Résumé du poste

Our client, a leading global pharmaceutical company with a significant presence in Polokwane, is seeking an experienced Senior Clinical Research Scientist to drive critical research and development efforts. This hybrid role involves designing, executing, and analyzing clinical trials to bring innovative therapies to market, shaping clinical strategies, and upholding high scientific standards.

Join a dedicated team engaged in advancing medical science and improving patient outcomes, with

Qualifications

• Ph.D. or Pharm.D. degree in a relevant scientific or medical discipline.
• Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical or biotechnology industry.
• Strong understanding of clinical trial design, execution, and data analysis.
• In-depth knowledge of Good Clinical Practice (GCP) and other relevant regulatory guidelines.
• Experience in manuscript writing and publication is highly desirable.

Responsabilités

• Design and develop clinical trial protocols, including study objectives, endpoints, and methodologies.
• Oversee the execution of clinical trials, ensuring compliance with regulatory requirements (e.g., GCP, ICH) and company standards.
• Analyze and interpret clinical trial data, contributing to comprehensive study reports and regulatory submissions.
• Collaborate with cross-functional teams, including regulatory affairs, medical affairs, biostatistics, and data management.
• Provide scientific and clinical expertise to support drug development programs.
• Identify and evaluate potential collaborators and key opinion leaders (KOLs) in relevant therapeutic areas.
• Contribute to the preparation of manuscripts for publication in peer-reviewed journals and presentations at scientific meetings.
• Monitor safety data and manage study-related issues.
• Stay abreast of scientific advancements, therapeutic trends, and competitive landscape within assigned therapeutic areas.

Connaissances

Clinical research

Communication

Independent work

Formation

Ph.D. or Pharm.D. degree

Description du poste

About the Role

Our client, a leading global pharmaceutical company with a significant presence in Polokwane , is seeking an experienced Senior Clinical Research Scientist to drive critical research and development efforts. This role involves designing, executing, and analyzing clinical trials to bring innovative therapies to market. You will play a pivotal role in shaping clinical strategies and ensuring the highest standards of scientific rigor. This position operates on a hybrid model, requiring regular engagement in our state-of-the-art facilities for essential team collaborations and hands‑on work, while offering flexibility for remote research and analysis. Join a dedicated team committed to advancing medical science and improving patient outcomes.

Key Responsibilities

• Design and develop clinical trial protocols, including study objectives, endpoints, and methodologies.
• Oversee the execution of clinical trials, ensuring compliance with regulatory requirements (e.g., GCP, ICH) and company standards.
• Analyze and interpret clinical trial data, contributing to comprehensive study reports and regulatory submissions.
• Collaborate with cross-functional teams, including regulatory affairs, medical affairs, biostatistics, and data management.
• Provide scientific and clinical expertise to support drug development programs.
• Identify and evaluate potential collaborators and key opinion leaders (KOLs) in relevant therapeutic areas.
• Contribute to the preparation of manuscripts for publication in peer-reviewed journals and presentations at scientific meetings.
• Monitor safety data and manage study-related issues.
• Stay abreast of scientific advancements, therapeutic trends, and competitive landscape within assigned therapeutic areas.

Requirements

• Ph.D. or Pharm.D. degree in a relevant scientific or medical discipline.
• Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical or biotechnology industry.
• Strong understanding of clinical trial design, execution, and data analysis.
• In-depth knowledge of Good Clinical Practice (GCP) and other relevant regulatory guidelines.
• Proven experience in a specific therapeutic area (e.g., oncology, cardiology, infectious diseases).
• Excellent written and verbal communication skills, with the ability to present complex scientific information effectively.
• Strong analytical and problem-solving skills.
• Ability to work independently and collaboratively within a hybrid work environment.
• Experience in manuscript writing and publication is highly desirable.

Benefits

• Competitive salary and annual bonus.
• Comprehensive health, dental, and vision coverage.
• Generous paid time off and company holidays.
• Retirement savings plan with company match.
• Opportunities for professional development and continuing education.
• Access to advanced research facilities and technologies.
• Supportive and collaborative work culture.
• Career advancement opportunities within a global organization.