Clinical Research Associate

Clinical Research Associate

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Qualifications

Clinical Research Associate needs 2-5 years of clinical research experience in industry settings with a bachelor's degree or higher in life sciences, health sciences, nursing, pharmacy, or other related field

Clinical Research Associate requires;

• oncology experience strongly preferred
• EDC systems
• Knowledge of clinical trial methodology as well as the drug research and development process
• Knowledge of GCP/ICH Guidelines for clinical studies

• ORACLE
• CLINICAL TRIALS
• CLINICAL MONITORING

Clinical Research Associate duties are:

• Participation in the evaluation of clinical trial site locations.
• Serving
  as the sponsor liaison to clinical sites during the activation process,
  as the study progresses, and during study close-out.
• Traveling to sites as necessary to conduct site qualification, initiation, and close-out (<10%).
• Collecting
  and managing regulatory documentation, to ensure compliance with GCP,
  ICH, regulatory authority, and ethics board requirements.
• Working
  with clinical site staff and investigators to obtain study data, ensure
  protocol compliance, and guarantee patient safety.
• Ensuring accurate and timely reporting of patient safety issues according to all relevant local and federal requirements.
• Participating in regional and global conference calls and meetings to review progress of ongoing clinical trials.
• Reviewing incoming clinical data, and preparing reports and presentations on the status of clinical studies.
• Helping to draft study manuals and protocol amendments as needed.
• Organizing and distributing study supplies and study-related documentation required for conduct of clinical trials.
• Coordinating
  the movement of laboratory samples between clinical sites and central
  laboratories, and tracking the status of samples and resulting
  laboratory data.

Additional Information

$31/HR

6 months