Senior Clinical Research Scientist

Placements24; Mbombela (Nelspruit); Hybrid; ZAR 1,200,000 - 1,800,000; Full time

Benefits offered by this job

Competitive salary

Healthcare benefits

Retirement plan

Professional growth

Job summary

Placements24 in Nelspruit seeks a Senior Clinical Research Scientist to lead trial design, execution, and interpretation. You will drive scientific rigor, collaborate with medical affairs and regulatory teams, and ensure high-quality study outputs.

The ideal candidate holds a Ph.D. or Master’s in a life science field and brings 5+ years in clinical research, with strong data analysis and GCP knowledge. This role offers growth and impact in a leading pharmaceutical environment in Nelspruit.

Qualifications

• Ph.D. or Master’s degree in a relevant life science or medical field (e.g., Medicine, Pharmacology, Biology, Pharmacy).
• Minimum 5 years of progressive experience in clinical research, preferably in pharma/biotech.
• Strong knowledge of clinical trial design, regulatory requirements, and data management.

Responsibilities

• Lead design and development of clinical trial protocols with regulatory alignment.
• Oversee execution of clinical trials from site initiation to close-out.
• Analyze and interpret trial data, including biostatistics.
• Prepare study reports, regulatory submissions, and publications.
• Collaborate with CROs, investigators, and regulatory authorities.
• Ensure compliance with GCP and relevant regulations.
• Provide scientific input to project teams and management.

Skills

Clinical research

Biostatistics

Regulatory affairs

GCP knowledge

Medical writing

Data analysis

Regulatory submissions

Communication skills

Education

Ph.D. or Master's degree in life sciences/medical field

Job description

About the Role

Our client, a leading pharmaceutical company focused on innovative therapies, is seeking a highly qualified Senior Clinical Research Scientist to join their team in **Nelspruit**. This critical role involves the design, execution, and interpretation of clinical trials, contributing significantly to the development of new medicines. The ideal candidate will possess a strong background in clinical research methodologies, data analysis, and regulatory affairs. You will work collaboratively with cross-functional teams, including medical affairs, regulatory, and development, to ensure the successful advancement of clinical programs. This position offers an exciting opportunity to impact patient care and contribute to cutting-edge medical advancements within a supportive and professional environment in **Nelspruit**.

Key Responsibilities

• Lead the design and development of clinical trial protocols, ensuring scientific rigor and alignment with regulatory requirements.
• Oversee the execution of clinical trials, from site selection and initiation to monitoring and close-out.
• Analyze and interpret clinical trial data, including statistical analysis and clinical interpretation.
• Prepare clinical study reports, regulatory submissions, and scientific publications.
• Collaborate with internal and external stakeholders, including investigators, clinical research organizations (CROs), and regulatory authorities.
• Ensure compliance with Good Clinical Practice (GCP) guidelines and other relevant regulations.
• Provide scientific and medical input to project teams and management.
• Stay abreast of the latest scientific advancements and clinical trends in relevant therapeutic areas.
• Contribute to the strategic planning of clinical development programs.

Requirements

• Ph.D. or Master's degree in a relevant life science or medical field (e.g., Medicine, Pharmacology, Biology, Pharmacy).
• Minimum of 5 years of progressive experience in clinical research, preferably within the pharmaceutical or biotechnology industry.
• Demonstrated experience in designing, executing, and managing clinical trials.
• Strong understanding of clinical trial methodology, biostatistics, and data management.
• Knowledge of regulatory requirements (e.g., FDA, EMA) and GCP guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong written and verbal communication skills, with the ability to present complex information effectively.
• Ability to work collaboratively in a multidisciplinary team environment in **Nelspruit**.

Benefits

• Competitive salary package with performance-based incentives.
• Comprehensive medical, dental, and vision insurance.
• Retirement savings plan and other financial wellness benefits.
• Opportunities for professional growth, training, and conference participation.
• A collaborative and supportive work culture in **Nelspruit**.
• The opportunity to contribute to life-changing medical advancements.