The Armauer Hansen Research Institute (AHRI) was founded in 1970 through the initiative of the Norwegian and Swedish Save the Children organizations seconded by the Ministry of Health of Ethiopia. The Institute got its name from the Norwegian physician, Gerhard Henrik Armauer Hansen, who first described the leprosy bacillus (Mycobacterium leprae). AHRI is a biomedical research institute that works in developing tools for prevention, control and treatment of mycobacterium and other diseases of public healthy importance through applied and basic biomedical research and training.
AHRI would like to hire qualified candidate in the position of Senior researcher
Position: Senior researcher
Responsibilities:
® Assumes central role in the development of various clinical research projects.
® Proposes plans, organizes and executes clinical research.
® Lead the clinical team in close collaboration with the PIs
® Provides technical and scientific guidance in the direction, planning, design, implementation, and interpretation of both investigator initiated and sponsor initiated trials
® Writes and secures grants and funding for clinical research and is responsible for controlling budgets.
® Plays a key role in development of clinical publication and communication strategies
® Develops and maintains collaborative relationships with key experts, investigators and institutions strategic to areas of interest
® Interacts with other scientists within and outside of the organization.
® Maintains knowledge as to developments and trends in applicable treatment landscape including current treatment strategies and new therapeutic developments
® Reports to clinical trial directorate
Requirements:
® The potential candidate should have Phd with 10years experience and 10 publication points.
® qualifications and competence in clinical research (advanced degree in clinical trials with clinical background preferred)
® prior experience in clinical trial industry serving as a professional in the conduct and management of clinical trials is advantageous
® Experience in writing study protocols and other technical documents
® Working knowledge of ICH-GCP, regulatory authority regulations, and other international and local and requirements for the conduct of clinical trials
® Strong background in literature review, protocol writing, data analysis and scientific report writing
® Demonstrated ability to communicate effectively and confidently with experts and/or opinion leaders in applicable fields