CenExel
Clinical Research Coordinator - Clinical Research
CenExel, Los Alamitos, California, us, 90721
Overview
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Clinical Research Coordinator - Clinical Research
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CenExel . CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise well-respected facilities with experience across Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Sites have in-patient capability, and the organization focuses on quality people, teamwork, and experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, CenExel Clinical Research provides competitive compensation and a generous benefits package to full-time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Insurance, and 401k. Schedule: Monday - Friday (08:00 am - 4:30 pm) Hourly Range: $30.00 - $36.00 (Depending on education, experience, and skillset) Job Summary
Responsible for assisting with coordinating clinical trials with adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies. Essential Responsibilities And Duties
Assists with coordinating all aspects of patient involvement from study initiation until study completion. Organizes research information for clinical trials. Observes subjects and assists with data analysis and reporting. Schedules the collection of data. Documents adverse events, protocol deviations, and other unanticipated problems appropriately. Reports research data to maintain quality and compliance. Performs administrative and regulatory duties related to the study as appropriate. Participates in other protocol development activities. Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.). Educates potential participants and caregivers on protocol specific details and expectations. Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned). Assumes other duties and responsibilities as assigned. Education/Experience/Skills
High school graduate or equivalent; Bachelor’s Degree preferred. 1+ years of experience as a Clinical Research Coordinator or similarly responsible position (Required). Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials. Strong leadership and mentorship skills. Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level. Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations. Works independently as well as functioning as part of a team. Must be able to effectively communicate verbally and in writing. Working Conditions
Indoor, Office environment. Shift work, depending on location. Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds. Reporting to work, as scheduled, is essential. Overnight travel may be required for training and/or investigative meetings. CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status. Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
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Join to apply for the
Clinical Research Coordinator - Clinical Research
role at
CenExel . CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise well-respected facilities with experience across Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Sites have in-patient capability, and the organization focuses on quality people, teamwork, and experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, CenExel Clinical Research provides competitive compensation and a generous benefits package to full-time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Insurance, and 401k. Schedule: Monday - Friday (08:00 am - 4:30 pm) Hourly Range: $30.00 - $36.00 (Depending on education, experience, and skillset) Job Summary
Responsible for assisting with coordinating clinical trials with adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies. Essential Responsibilities And Duties
Assists with coordinating all aspects of patient involvement from study initiation until study completion. Organizes research information for clinical trials. Observes subjects and assists with data analysis and reporting. Schedules the collection of data. Documents adverse events, protocol deviations, and other unanticipated problems appropriately. Reports research data to maintain quality and compliance. Performs administrative and regulatory duties related to the study as appropriate. Participates in other protocol development activities. Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.). Educates potential participants and caregivers on protocol specific details and expectations. Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned). Assumes other duties and responsibilities as assigned. Education/Experience/Skills
High school graduate or equivalent; Bachelor’s Degree preferred. 1+ years of experience as a Clinical Research Coordinator or similarly responsible position (Required). Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials. Strong leadership and mentorship skills. Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level. Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations. Works independently as well as functioning as part of a team. Must be able to effectively communicate verbally and in writing. Working Conditions
Indoor, Office environment. Shift work, depending on location. Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds. Reporting to work, as scheduled, is essential. Overnight travel may be required for training and/or investigative meetings. CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status. Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
#J-18808-Ljbffr