crc.

We are looking for an experienced CRC (clinical study coordinator). If you’re dedicated and ambitious, the role of CRC is an excellent place to grow your career. 

Do you have at least 2 years of experience in clinical research field? Then don’t hesitate to apply for the role of CRC.

Whatever your career goals, we are here to help you build a smart and flexible career with no limits! Read below and apply now!!! 

benefits

Some of the advantages you can expect from your role as a CRC are:

• A competitive compensation package is provided
• Consistent workload
• Career development opportunities 

responsibilities

As a CRC, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract.

Primary Responsibilities

• Participation in training.
• Familiarization and compliance with studies core documents (e.g. protocol), processes and timelines.
• Work with the Principal Investigator (PI) to develop and implement recruitment strategies in accordance with the study requirements.
• Assist PI in assuring that all site investigational team members have met training requirements in accordance with the protocol, policies and procedures.
• Maintain effective and ongoing communication with the sponsor, the PI and the site’s investigational team during the course of the study.
• Pre-screen study subjects for eligibility, as instructed by the study protocol, coordinates subjects assessments and other study evaluations (e.g. central laboratories documentation and processes).
• Assure timely completion of subjects (e)CRFs.
• Assist investigational sites with IRB/IEC submissions and ensures collection of required essential documents for study start-up, regulatory submissions as well as throughout the conduct of the study.
• Maintain adequate inventory of study supplies (medication and non-drug supplies). If handling investigational drugs/devices, follows the sponsor protocol and investigational drug accountability.
• Maintain study files and records in accordance with sponsor requirements.

…