What are the responsibilities and job description for the URGENT CRC Manager position at Actalent?
URGENT CRC MANAGER NEEDED
Description:
The Manager of CRC Clinical Research works with a team of managers and the Director of the Cancer Clinical Trials Office (CCTO) to oversee a team of CRCs while performing high-level cancer clinical trials, all phases. The Manager of CRC Clinical Research aligns with the strategic goal to transform the practice of clinical research and the operational goal to strengthen clinical trials. RUMC will be a national leader in the conduct of multi-center clinical trials. The CCTO will be a hub to connect study teams to the resources they need within the institution in addition to interacting with sponsors. Provides work direction, education, orientation, and operational problem solving within the work unit on a day-to-day basis and communicates and coordinates activities with management. The individual who holds this position exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
JOB DESCRIPTION:
- Manages Clinical Research Nurses, Clinical Research Coordinators, Regulatory Coordinators, Clinical Research Analysts, and other study-specific staff within CCTO that supports the Cancer Center.
- Receives requests for CRNs, CRCs, and RCs and make assignments of available staff.
- Provides day-to-day supervision, ensures milestone attainment, and communicates metrics effectively.
- Assists the Director in implementing and executing business strategies and measuring performance toward goals.
- Collaborates with Principal Investigators and other members of clinical research teams while providing excellent customer service.
- Stays current with industry trends; summarizes and share relevant industry information during internal and external presentations.
- Coordinates the training activities of all clinical research personnel across the Cancer Center.
- Works with study staff, data management teams, and Clinical Research Assistants to ensure efficient data collection and quality assurance procedures are in place.
- Assists with problem solving activities to bring smooth resolutions.
- Fills in for Clinical Research Coordinators and related functions during unexpected absences.
- Performs other job-related assignments as required.
Skills Needed:
- Clinical trial experience
- Oncology, cardiology, neurology, or orthopedic CLINICAL EXPERINCE
- Clinical Study Management experience
- EPIC, Medidate Rave, Redcap experience
- Regulatory and coordinating experience
- 3-7 years if CRC experience in Oncology, Cardiology Neurology, or Orthopedic therapeutic areas
- 3-7 years of CRC, CRN, or Regulatory Management experience
Additional Skills & Qualifications:
- Bachelor's degree.
- Five years of clinical research experience with three years of supervisory experience.
- Outstanding computer skills.
- Excellent organizational and interpersonal skills.
- Demonstrated commitment to clinical research.
- Ability to understand and maintain discretion and confidentiality related to all aspects of the trial.
- Ability to work with a variety of individuals in a professional manner.
- Availability on some evenings and occasional Saturdays when needed.
If interested please reach out to Sarah at sacollins@actalentservices.com or 312.601.3614
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Description:
The Manager of CRC Clinical Research works with a team of managers and the Director of the Cancer Clinical Trials Office (CCTO) to oversee a team of CRCs while performing high-level cancer clinical trials, all phases. The Manager of CRC Clinical Research aligns with the strategic goal to transform the practice of clinical research and the operational goal to strengthen clinical trials. RUMC will be a national leader in the conduct of multi-center clinical trials. The CCTO will be a hub to connect study teams to the resources they need within the institution in addition to interacting with sponsors. Provides work direction, education, orientation, and operational problem solving within the work unit on a day-to-day basis and communicates and coordinates activities with management. The individual who holds this position exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
JOB DESCRIPTION:
- Manages Clinical Research Nurses, Clinical Research Coordinators, Regulatory Coordinators, Clinical Research Analysts, and other study-specific staff within CCTO that supports the Cancer Center.
- Receives requests for CRNs, CRCs, and RCs and make assignments of available staff.
- Provides day-to-day supervision, ensures milestone attainment, and communicates metrics effectively.
- Assists the Director in implementing and executing business strategies and measuring performance toward goals.
- Collaborates with Principal Investigators and other members of clinical research teams while providing excellent customer service.
- Stays current with industry trends; summarizes and share relevant industry information during internal and external presentations.
- Coordinates the training activities of all clinical research personnel across the Cancer Center.
- Works with study staff, data management teams, and Clinical Research Assistants to ensure efficient data collection and quality assurance procedures are in place.
- Assists with problem solving activities to bring smooth resolutions.
- Fills in for Clinical Research Coordinators and related functions during unexpected absences.
- Performs other job-related assignments as required.
Skills Needed:
- Clinical trial experience
- Oncology, cardiology, neurology, or orthopedic CLINICAL EXPERINCE
- Clinical Study Management experience
- EPIC, Medidate Rave, Redcap experience
- Regulatory and coordinating experience
- 3-7 years if CRC experience in Oncology, Cardiology Neurology, or Orthopedic therapeutic areas
- 3-7 years of CRC, CRN, or Regulatory Management experience
Additional Skills & Qualifications:
- Bachelor's degree.
- Five years of clinical research experience with three years of supervisory experience.
- Outstanding computer skills.
- Excellent organizational and interpersonal skills.
- Demonstrated commitment to clinical research.
- Ability to understand and maintain discretion and confidentiality related to all aspects of the trial.
- Ability to work with a variety of individuals in a professional manner.
- Availability on some evenings and occasional Saturdays when needed.
If interested please reach out to Sarah at sacollins@actalentservices.com or 312.601.3614
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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