As part of our dynamic team, the Scientific Officer will contribute to the conception, oversight, and coordination of various scientific aspects in clinical research. The expertise will support the Chief Scientific Officer (CSO) in project planning, management, grant applications, and represent our company at high-level conferences and similar events.
Key Performance Areas (KPA’s) & Responsibilities includes, but not limited to:
Trial and Grant Management
- Provide strategic scientific and medical guidance across clinical trials, ensuring protocol adherence, regulatory compliance (FDA, SAHPRA, etc.), and ethical standards.
- Collaborate with investigators, project teams, and site staff for effective trial execution, addressing protocol deviations, safety, and compliance issues.
- Provide mentorship and capacity development opportunities to investigators and supporting teams.
- Support or lead grant applications, funding management, and project reporting requirements, coordinating closely with the Chief Science Officer (CSO).
- Design and refine trial protocols, study methodologies, and ensure Good Clinical Practice (GCP) alignment, actively engaging in risk assessments and safety monitoring.
- Coordinate internal meetings to discuss project updates and problem-solving and contribute to the continuous improvement of trial processes.
Dissemination and Stakeholder Engagement
- Oversee dissemination activities, including the preparation of scientific manuscripts, presentations, and reports for conferences and publication.
- Build and maintain professional relationships with key stakeholders, including sponsors, partners, state representatives, and research collaborators.
- Represent the organisation at national and international scientific meetings, courses, and conferences, acting as a spokesperson on scientific initiatives when required.
Ideal Requirements
- MBChB and HPCSA registration
- A masters or PhD in healthcare or similar qualification is advantageous.
- At least 2 years of experience in clinical research, and relevant qualification (Good Clinical Practice) in clinical research.
- A good understanding of science and research methodology
- Grant and protocol writing experience is advantageous.
- A special interest and preferably some experience in TB research.
Key Personal Inherent Characteristics
- Strong interpersonal skills.
- An excellent communicator, verbal, written and listening, with all relevant stakeholders.
- Strong influencing skills, team leader.
- Demonstrates company culture, values and core competencies.
- Scientific English fluency.
Details:
Area: Parow
Contract Type: Permanent
Applications Close: 22 November 2024 at 11h00
Please indicate in your application that you are applying for the above-mentioned position.
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