Clinical Studies Manager – CTM

The Company is an established midsized High-Tech Startup, located in Herzliya. We are a warm and caring group, with a lively spirit.
We are looking for a responsible clinical studies manager to oversee a number of parallel clinical trials (Local and abroad)
Responsibilities and Duties:
· Conduct a variety of clinical trial.
· Helsinki / IRB / ethics committee approval
· Oversee pre-clinical trial.
Qualifications:
· MD or master’s in medical/Bio Studies
· Proven work experience as a clinical study manager / relevant role
· CRA and GCP approved.
· Strong sense of responsibility and ability to complete tasks with minimal supervision
· High proficiency in English (Fluent/Mother-tongue/Native speaker)
· Proven work experience with CRM software and MS Office
· Excellent listening, verbal, negotiation and presentation skills
· Strong verbal, presentation and written communication skills
· Discretion and trustworthiness: you will often be party of confidential information
Reports To
The clinical studies manager will report to the CEO and work together with the Executive team.
Working Hours
The general office hours are from 09:00-18:00, while urgent matters will require working throughout some evenings and occasionally a couple of hours over the weekend.