Sr. CRA / Senior Clinical Research Associate

IRW is expanding and therefore looking for Sr.CRA;s


Qualifications and background needed:

Bachelor or Masters degree in life sciences, pharmacy or nursing.
Preferably a minimum of 4 years of clinical research experience in the Pharmaceutical/CRO industry Experience of Clinical Trial Project Management.
High level of quality consciousness.
Well organized and adaptive to change.
Acts responsibly
Strong interpersonal skills.
Good ability to express oneself.
Good knowledge of spoken and written English.
Organizational skills.
Ability to work independently.
Ability to priorities and handle several tasks simultaneously.
Understanding for customer care and business development.
Valid driving license.


Main Responsibilities:

Prepare and complete applications
Responsible for completion of study documentation.
Preparing Manuals.
Responsible for the sites and on-site monitoring, management and reporting throughout the studies.
Participate in Audits, Inspections, etc.
Assist in clean file procedures
Prepare and conduct study activities.
Selecting and negotiating contracts.
Planning and participating at Investigators meeting
Demonstrate willingness to take on any level project activity in support of study delivery.