Senior Clinical Research Scientist

Placements24; Mtubatuba Local Municipality; Hybrid; ZAR 900.000 - 1.300.000; Vollzeit

Benefits dieser Stelle

Health insurance

Annual leave and paid sick days

Professional development

Conference attendance

Retirement plan

Zusammenfassung

Placements24 is seeking a Senior Clinical Research Scientist to join our Richards Bay team, KwaZulu-Natal, leading the design and oversight of clinical trials for novel therapies. You will ensure scientific integrity, ethics, and regulatory compliance from protocol development through data analysis and reporting.

The role requires a PhD or MSc, 7+ years in clinical research focusing on trial design and management, and strong collaboration with R&D, regulatory, and medical affairs teams.

Qualifikationen

• Experience in study protocol development and trial design.
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
• Proven ability to manage multi-center clinical trials.
• Excellent written and verbal communication and presentation skills.

Aufgaben

• Lead the development and refinement of clinical trial protocols.
• Oversee operational execution, timelines, budgets, and resources.
• Ensure compliance with GCP, ICH guidelines, and regulatory requirements.
• Collaborate with investigators and internal teams to ensure safety and data integrity.
• Analyze data and contribute to study reports and regulatory submissions.
• Manage relationships with CROs and external vendors.
• Provide scientific expertise to study teams throughout the trial lifecycle.
• Identify and evaluate new clinical research opportunities.
• Stay updated with literature, trends, and regulatory changes.
• Deliver scientific presentations to stakeholders.

Kenntnisse

Clinical research

Project management

Communication skills

Data analysis

Ausbildung

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

Jobbeschreibung

About the Role

Our client, a global leader in innovative healthcare solutions, is seeking a highly qualified Senior Clinical Research Scientist to join their expanding team in Richards Bay, KwaZulu-Natal . This crucial role will involve the design, implementation, and oversight of clinical trials for novel therapeutic agents. You will be instrumental in ensuring the scientific integrity, ethical conduct, and regulatory compliance of these studies, from protocol development through to data analysis and reporting. The ideal candidate will possess extensive experience in clinical research methodology, a strong understanding of medical science, and exceptional project management skills. This position offers a unique opportunity to contribute to the development of life-saving treatments and to work within a dynamic and forward-thinking organization. We are committed to fostering an environment where scientific excellence and patient well-being are paramount. The successful applicant will have a significant impact on advancing medical knowledge and improving patient outcomes. This role requires a deep commitment to scientific rigor and ethical research practices.

Key Responsibilities

• Lead the development and refinement of clinical trial protocols, ensuring scientific validity and alignment with regulatory requirements.
• Oversee the operational execution of clinical trials, managing timelines, budgets, and resources effectively.
• Ensure compliance with Good Clinical Practice (GCP), regulatory guidelines (e.g., ICH, FDA, EMA), and institutional policies.
• Collaborate with investigators, site staff, and internal teams to ensure patient safety and data integrity.
• Analyze and interpret clinical trial data, contributing to study reports, publications, and regulatory submissions.
• Manage relationships with Contract Research Organizations (CROs) and other external vendors.
• Provide scientific and technical expertise to study teams, guiding decision-making throughout the trial lifecycle.
• Contribute to the identification and evaluation of new clinical research opportunities and potential therapeutic areas.
• Stay current with scientific literature, industry trends, and regulatory changes relevant to clinical research.
• Prepare and deliver scientific presentations to internal stakeholders and external audiences.

Requirements

• Ph.D. or Master's degree in a relevant life science, health science, or medical field.
• A minimum of 7 years of experience in clinical research, with a significant portion focused on clinical trial design and management.
• Demonstrated expertise in study protocol development, statistical analysis plans, and clinical study reports.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Proven experience in managing multi-center clinical trials, preferably in relevant therapeutic areas.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent communication, interpersonal, and presentation skills.
• Ability to effectively manage projects, timelines, and budgets.
• Experience working with cross-functional teams, including R&D, regulatory affairs, and medical affairs.
• A proactive and detail-oriented approach to work.

Benefits

• An annual salary ranging from R to R , dependent on experience and qualifications.
• Comprehensive health insurance, including medical, dental, and vision coverage.
• Generous annual leave and paid sick days.
• Opportunities for professional development, including training programs and conference attendance.
• Exposure to cutting-edge therapies and innovative research projects.
• Performance-based bonuses and incentives.
• A supportive and collaborative work environment dedicated to improving patient lives.
• Company-sponsored retirement plan.