Insight Global
Our client is looking for a clinical research data coordinator to work five days on site at their facility. The daily responsibilities will include:
Support the daily activities of early phase oncology clinical trials. Ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. Data collection, and maintaining compliance with Good Clinical Practice (GCP). Communicate on a regular basis with Study Sponsors, CROs, staff, etc. regarding questions, concerns, as well as status of the protocol. Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study. Maintain files using standardized study document labeling and filing procedures.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal. com. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/. Hands-on experience with clinical trial software (e. g., CTMS, EDC systems, Oncore) Strong understanding of GCP, clinical trial protocols, and regulatory compliance Prior experience in early-phase oncology trials Familiarity with sponsor and CRO communications Knowledge of IRB processes and regulatory documentation Experience with electronic data capture systems and clinical trial management platforms is a plus 13 years of master data management experience, preferably in a clinical research setting Strong written and verbal communication Detail oriented
Support the daily activities of early phase oncology clinical trials. Ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. Data collection, and maintaining compliance with Good Clinical Practice (GCP). Communicate on a regular basis with Study Sponsors, CROs, staff, etc. regarding questions, concerns, as well as status of the protocol. Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study. Maintain files using standardized study document labeling and filing procedures.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal. com. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/. Hands-on experience with clinical trial software (e. g., CTMS, EDC systems, Oncore) Strong understanding of GCP, clinical trial protocols, and regulatory compliance Prior experience in early-phase oncology trials Familiarity with sponsor and CRO communications Knowledge of IRB processes and regulatory documentation Experience with electronic data capture systems and clinical trial management platforms is a plus 13 years of master data management experience, preferably in a clinical research setting Strong written and verbal communication Detail oriented