Clinical Research Coordinator - 253040 (Indianapolis)
Medix™, Indianapolis, IN, United States
Role
: Clinical Research Coordinator - 5 month Contract assignment, 24 hours a week
Location
: Onsite - Indianapolis, IN 46202
Relocation candidates will NOT be considered for this position
Role is
100% onsite,
there is no opportunity for hybrid or remote work at this time
Therapeutic Area
:
Oncology
Employment Type
: Position is a contract, project based support role - current contract duration is estimated to be 5 months, possibility for extension depending on project needs
Schedule/ Shift:
Part time, 24 hours a week
M-F during daytime business hours - NO evenings/weekends, open to reviewing candidates' preferred schedules
Responsibilities / Job Duties:
We are seeking a detail-oriented, part time Clinical Research Coordinator (CRC) with demonstrated experience in oncology clinical trials and a strong focus on data management and electronic data capture (EDC). This role is ideal for candidates who excel in high-volume data entry, rigorous data verification, proactive query resolution, and consistent participant follow-up within a fast-paced research environment.
The CRC will be responsible for:
Accurate and timely EDC data entry, ongoing data review, and source data verification to ensure completeness, consistency, and protocol compliance
Proactive query generation and resolution, including collaboration with sponsors, monitors, and internal teams to address discrepancies and maintain data integrity
Managing and maintaining high-quality clinical trial data across multiple EDC platforms
Conducting participant follow-up activities, including visit coordination, data collection, and ensuring adherence to study protocols—particularly within oncology studies
Supporting oncology trial operations, including tracking adverse events, concomitant medications, and protocol-specific endpoints
Demonstrating hands-on experience with multiple EDC systems—such as Medidata Rave, Oracle InForm, Oracle Clinical, Veeva Vault, or similar—showing adaptability and cross-platform proficiency
(Note: Experience limited to a single system, such as REDCap alone, will not be sufficient for this role.)
This position plays a critical role in ensuring data accuracy, regulatory compliance, and audit readiness. The ideal candidate is highly organized, detail-driven, and proactive, with a strong commitment to data quality and patient-centered research—especially in oncology settings.
: Clinical Research Coordinator - 5 month Contract assignment, 24 hours a week
Location
: Onsite - Indianapolis, IN 46202
Relocation candidates will NOT be considered for this position
Role is
100% onsite,
there is no opportunity for hybrid or remote work at this time
Therapeutic Area
:
Oncology
Employment Type
: Position is a contract, project based support role - current contract duration is estimated to be 5 months, possibility for extension depending on project needs
Schedule/ Shift:
Part time, 24 hours a week
M-F during daytime business hours - NO evenings/weekends, open to reviewing candidates' preferred schedules
Responsibilities / Job Duties:
We are seeking a detail-oriented, part time Clinical Research Coordinator (CRC) with demonstrated experience in oncology clinical trials and a strong focus on data management and electronic data capture (EDC). This role is ideal for candidates who excel in high-volume data entry, rigorous data verification, proactive query resolution, and consistent participant follow-up within a fast-paced research environment.
The CRC will be responsible for:
Accurate and timely EDC data entry, ongoing data review, and source data verification to ensure completeness, consistency, and protocol compliance
Proactive query generation and resolution, including collaboration with sponsors, monitors, and internal teams to address discrepancies and maintain data integrity
Managing and maintaining high-quality clinical trial data across multiple EDC platforms
Conducting participant follow-up activities, including visit coordination, data collection, and ensuring adherence to study protocols—particularly within oncology studies
Supporting oncology trial operations, including tracking adverse events, concomitant medications, and protocol-specific endpoints
Demonstrating hands-on experience with multiple EDC systems—such as Medidata Rave, Oracle InForm, Oracle Clinical, Veeva Vault, or similar—showing adaptability and cross-platform proficiency
(Note: Experience limited to a single system, such as REDCap alone, will not be sufficient for this role.)
This position plays a critical role in ensuring data accuracy, regulatory compliance, and audit readiness. The ideal candidate is highly organized, detail-driven, and proactive, with a strong commitment to data quality and patient-centered research—especially in oncology settings.