protocols, standard operating procedures (SOP), good clinical practices (GCP), and regulatory requirements.
Develop and maintain relationships with clinical investigators, medical educators, clinical research organizations (CRO), hospitals, and research institutions to initiate and expedite clinical studies.
Review adverse event cases with investigators, monitor timelines, prepare study documents, and issue status reports.
Plan and conduct Site Selection Visits (SSVs) as well as collect and archive site documents.
Prepare and conduct Site Initiation Visits (SIVs), as well as coordinate shipments to sites with required trial supplies.
Develop and maintain relationships with clinical investigators, medical educators, clinical research organizations (CRO), hospitals, and research institutions to initiate and expedite clinical studies.
Review adverse event cases with investigators, monitor timelines, prepare study documents, and issue status reports.
Plan and conduct Site Selection Visits (SSVs) as well as collect and archive site documents.
Prepare and conduct Site Initiation Visits (SIVs), as well as coordinate shipments to sites with required trial supplies.
Requirements:
Bachelor’s degree in a Life Science, Pharmacy, Nursing qualification or equivalent.
2-3 years of experience in overseeing clinical trials and ensuring compliance with regulatory requirements.Knowledge of protocols, SOPs, GCP, and other applicable regulatory guidelines.
Strong communication and interpersonal skills to build and maintain relationships with stakeholders.
Good planning and organizational skills, project management skills, and proven excellence in the conduct of clinical trial activities from monitoring to the management of multinational trials.
IT proficiency: MS Office, clinical trials systems (e.g., COSMOS, IWRS, ePRO, NovoTime, CONNECT, HOT, Veeva)
Attention to detail and ability to work in a fast-paced environment.
Our offices located in Kfar Saba. This is a hybrid position which requires your presence in the office three days a week.
Fluency in Hebrew and English.
Bachelor’s degree in a Life Science, Pharmacy, Nursing qualification or equivalent.
2-3 years of experience in overseeing clinical trials and ensuring compliance with regulatory requirements.Knowledge of protocols, SOPs, GCP, and other applicable regulatory guidelines.
Strong communication and interpersonal skills to build and maintain relationships with stakeholders.
Good planning and organizational skills, project management skills, and proven excellence in the conduct of clinical trial activities from monitoring to the management of multinational trials.
IT proficiency: MS Office, clinical trials systems (e.g., COSMOS, IWRS, ePRO, NovoTime, CONNECT, HOT, Veeva)
Attention to detail and ability to work in a fast-paced environment.
Our offices located in Kfar Saba. This is a hybrid position which requires your presence in the office three days a week.
Fluency in Hebrew and English.
This position is open to all candidates.
