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The University of Chicago
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Chicago, Illinois
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Investigator (PI) and
under the direction of the Section Administrator and/or Clinical
Research Manager within ... Investigator is
primarily responsible for the overall design, conduct, and management of
the clinical trial
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US Tech Solutions
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Malden, Massachusetts
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coordination of the daily clinical trial activities and plays a critical role in the conduct of the study ... :**
Manages and oversees the day-to-day operations in the administration of clinical trial activities at the
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US Tech Solutions
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River Forest, Illinois
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coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The ... , train, demonstrate and lead clinical trial team members in the implementation of trial related
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US Tech Solutions
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Atlantic City, New Jersey
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coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The ... , train, demonstrate and lead clinical trial team members in the implementation of trial related
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US Tech Solutions
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North Las Vegas, Nevada
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coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The ... , train, demonstrate and lead clinical trial team members in the implementation of trial related
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US Tech Solutions
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Chicago, Illinois
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coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The ... , train, demonstrate and lead clinical trial team members in the implementation of trial related
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US Tech Solutions
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Humble, Texas
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coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The ... , train, demonstrate and lead clinical trial team members in the implementation of trial related
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US Tech Solutions
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Atlantic City, New Jersey
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coordination of the daily clinical trial activities and plays a critical role in the conduct of the study ... :**
Manages and oversees the day-to-day operations in the administration of clinical trial activities at the
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ICONMA, LLC
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United States
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the oversight, facilitation and coordination of the daily clinical trial activities and plays a ... . The Sr. CRC is expected to support, guide, train, demonstrate and lead clinical trial team members in
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Actalent
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Overland Park, Kansas
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interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol.
• Creates standard operating procedures
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Actalent
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Chicago, Illinois
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administration of clinical trial activities at the site-level (i.e., direct interactions with study participants).
• Regularly interfaces with current and potential clinical trial participants to determine eligibility and
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Actalent
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Las Vegas, Nevada
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-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants).
• Regularly interfaces with current and potential clinical trial
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Actalent
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Overland Park, Kansas
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-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants).
• Regularly interfaces with current and potential clinical trial
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Actalent
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Atlantic City, New Jersey
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interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol.
• Creates standard operating procedures
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Actalent
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Oak Park, Illinois
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interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol.
• Creates standard operating procedures
...
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Actalent
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Houston, Texas
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administration of clinical trial activities at the site-level (i.e., direct interactions with study participants).
• Regularly interfaces with current and potential clinical trial participants to determine eligibility and
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Actalent
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Atlantic City, New Jersey
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administration of clinical trial activities at the site-level (i.e., direct interactions with study participants).
• Regularly interfaces with current and potential clinical trial participants to determine eligibility and
...
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Actalent
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Las Vegas, Nevada
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interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol.
• Creates standard operating procedures
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Actalent
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North Las Vegas, Nevada
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and oversees the day-to-day operations in the administration of clinical trial activities at the site ... potential clinical trial participants to determine eligibility and consent of study participants in
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Actalent
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Houston, Texas
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-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants).
• Regularly interfaces with current and potential clinical trial
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Actalent
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Malden, Massachusetts
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interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol.
• Creates standard operating procedures
...
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Actalent
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Atlantic City, New Jersey
...
-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants).
• Regularly interfaces with current and potential clinical trial
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University of Maryland, Baltimore
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Baltimore, Maryland
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more research studies or clinical trial protocols. The position coordinates data collection and ... ./ * *PRIMARY DUTIES * Independently manages operations of two or more research studies or clinical trial
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UCLA Health
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Marina Del Rey, California
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operational management of clinical research/trial/study activities from design, set up, conduct, through ... and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial
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Actalent
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Malden, Massachusetts
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day-to-day operations in the administration of clinical trial activities at the site-level (i.e ... clinical trial participants to determine eligibility and consent of study participants in alignment with
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US Tech Solutions
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Overland Park, Kansas
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clinical trial space.
Skills:
Proficiency in ICH-GCP, US CFR, and HIPAA ... support or temporary coverage as needed.
Responsibilities:
Conducting all trial
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US Tech Solutions
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Pearland, Texas
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clinical trial space.
Skills:
Proficiency in ICH-GCP, US CFR, and HIPAA ... support or temporary coverage as needed.
Responsibilities:
Conducting all trial
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US Tech Solutions
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Las Vegas, Nevada
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support or temporary coverage as needed.
Responsibilities:
Conducting all trial visits ... query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate
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US Tech Solutions
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Oak Park, Illinois
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clinical trial space.
Skills:
Proficiency in ICH-GCP, US CFR, and HIPAA ... support or temporary coverage as needed.
Responsibilities:
Conducting all trial
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US Tech Solutions
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Kansas City, Missouri
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coordination of the daily clinical trial activities and plays a critical role in the conduct of the study ... , guide, train, demonstrate and lead clinical trial team members in the implementation of trial related
...
