Scorpion Therapeutics
Sr CRA - Oncology - FSP - North Central & West Coast
Scorpion Therapeutics, Saint Paul, Minnesota, United States
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JobsAI . Role Summary
Sr CRA - Oncology - FSP - North Central & West Coast Responsibilities
Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned - Responsible for all aspects of site management as prescribed in the project plans General On-Site Monitoring Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management Assist with training of new employees, eg. co-monitoring Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned Perform other duties as assigned by management Qualifications
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) 3+ years of onsite Clinical Monitoring experience Oncology experience required Open to major hub locations in the Northeast US Skills
Fast paced environment adaptability Attention to protocol adherence and quality timelines Teamwork and strong interpersonal skills Technology proficiency with electronic data capture Education
Not specified Additional Requirements
Travel to client sites; domestic and international travel may be required Physical requirements include sitting for extended periods, lifting up to 15-20 lbs, and frequent computer use
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JobsAI . Role Summary
Sr CRA - Oncology - FSP - North Central & West Coast Responsibilities
Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned - Responsible for all aspects of site management as prescribed in the project plans General On-Site Monitoring Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management Assist with training of new employees, eg. co-monitoring Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned Perform other duties as assigned by management Qualifications
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) 3+ years of onsite Clinical Monitoring experience Oncology experience required Open to major hub locations in the Northeast US Skills
Fast paced environment adaptability Attention to protocol adherence and quality timelines Teamwork and strong interpersonal skills Technology proficiency with electronic data capture Education
Not specified Additional Requirements
Travel to client sites; domestic and international travel may be required Physical requirements include sitting for extended periods, lifting up to 15-20 lbs, and frequent computer use
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