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| Clinical Sciences | Full-time
,We are currently seeking an Associate Director, Clinical Sciences to join the R&D department. The Associate Director, Clinical Sciences will provide clinical pharmacology/sciences expertise to the development of innovative medicines in the MMV portfolio to cure and protect vulnerable and under-served populations at risk of malaria.
The Associate Director, Clinical Sciences will:
- Define the overall clinical development strategy and corresponding study designs that best deliver the data supporting the target product profile ensuring relevant internal and external expert function inputs on cross-functional project teams
- Provide analysis of emerging study data and to recommend to the Project Director any needed changes to project strategy
- Conduct study data review and interpretation to ensure data-driven recommendations to MMV management as part of the project team, e.g. for transition to next phase
- Work closely with the counterpart from Pharmaceutical Partner on the joint clinical team to provide aligned recommendations and to support the Project Directors
- Contribute to the development of clinical documents as required including clinical study protocols, investigator brochures and other regulatory documents
- Present information internally and externally to multiple stakeholders
- Work closely with clinical operations during study set-up, conduct and close-out activities, and act as clinical sciences subject matter expert to study sites
Education and experience:
- PhD in the field of clinical pharmacology, biological sciences or PharmD degree
- Minimum 5-8 years clinical scientist experience in a pharmaceutical/biotech industry, academia, or non-profit organizations
- Experience in late stage drug development and field studies, particularly in infectious diseases would be an asset
- Experience in drug combination development, medicines for pediatric population or pregnant women, would be an asset
- Experience with multi-disciplinary team model in the work environment
Technical skills required:
- Expert knowledge of clinical pharmacology, pharmacokinetics
- Familiarity with principles of biostatistics, epidemiology, PKPD modelling
- Knowledge of regulatory authorities and global health bodies requirements
- Knowledge of ICH Good Clinical Practice standards
- Excellent technical writing skills
- Proficient English (oral and written); French and/or Portuguese would be an asset
Behavioural skills required:
- Motivated and passionate about MMV’s Mission
- Scientific leadership skills
- Team player and a strong collaborator
- Ability to influence and act as a role model for others
- Strong communication skills, verbal and written
- Results-focused; with good project management, multi-tasking and organisational skills
- Demonstrate flexibility, dedication, and follow through to completion
- Willingness to travel, including endemic countries when appropriate
Start date: 15 March 2021
Interested applicants should send their CV and a cover letter giving reasons for their interest in the position before 31st December 2020.