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Senior CRA and CRA II

Zoek Pin Pakhru-in, Kangra, Himachal Pradesh


Permanent (Full time)

Posted 13 days ago

The Role Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness Dependent on level of experience you may assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects What you need Minimum 12-18 months of independent monitoring experience in phase I-III trials as a CRA for a pharmaceutical or CRO organization (for a Senior role at least 36 months experience is required). Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data You will possess excellent written and verbal communication in English Ability to produce accurate work to tight deadlines within a pressurized environment You will be available to travel at least 70 PERCENT of the time (domestic -fly and drive) and should possess a valid driving license

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