Sr. Clinical Study Coordinator
2 weeks ago
Piper
Companies
is currently seeking a Sr. Clinical Study Coordinator
to support a growing and innovative Clinical Research Organization.
This role is a 100 percent remote opportunity. The Sr. Clinical Study Coordinator
will support quality control review and data entry activities during CRF tracking.
Responsibilities of Sr. Clinical Study Coordinator
•Ensure data analysis and validation meet regulatory standards and enhance study effectiveness.
•Collaborate with various teams to ensure timely submission of data and documentation to regulatory agencies.
•Aid in resolving site data queries and addressing safety concerns promptly.
•Identify and resolve issues related to subject recruitment and data quality in a proactive manner.
•Work closely with Sponsor Data Management and Clinical Science teams when necessary.
•Stay updated on study events and requirements, actively participating in meetings and audits.
Qualifications of the Sr. Clinical Study Coordinator
•A minimum of 2 years of clinical experience
•Familiarity with clinical trials, regulations, and IRB requirements
•Proficient in computer databases and the Microsoft Office suite.
•Capable of managing large volumes of information, prioritizing tasks effectively, and collaborating within study teams or working independently.
•Bachelor of Science degree in a scientific discipline from an accredited college or university is strongly preferred.
Compensation for the Sr. Clinical Study Coordinator
•Pay Rate: $25-30/hr.
•Contract (with Possible Extension/Conversion)
•Comprehensive Benefits package: Medical, Dental, Vision, 401K, PTO
Keywords: Clinical Research, Clinical Research Coordinator, CRC, CTA, Clinical Data, Clinical Trials, IRB, Oncology, TMF, eTMF,
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