$26.75 - 35.5 hourly
Number of Applicants
:000+
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We are currently staffing a Clinical Research Coordinator for one of New York's leading Medical Care company. APPLY NOW to find out more.
Description: Under supervision, the clinical research coordinator will assist in carrying out research activities related to clinical research and laboratory/translational research. In addition, they will be given the opportunity to enhance their research skills by working with our diverse team of researchers.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
• In collaboration with the PI, incorporates clinical judgment and knowledge of protocol to identify potential study participants according to inclusion and exclusion criteria.
• Obtains informed consent according to GCP.
• Schedules subject visits.
• Prepares labs/tests per protocol.
• Monitors and evaluates patients’ condition with regard to the investigational product.
• Conducts routine assessments to evaluate the subject’s response to investigational product, and communicates observations to the PI, sponsor and IRB as appropriate.
• Meets with the study monitor to review, verify and correct all data entered onto the case report form and to ensure appropriate maintenance of study records.
• Reports subject’s progress, complaints and issues to PI, study sponsor, or IRB as needed in a timely manner.
• Conducts ongoing assessments of the overall study execution within the facility/practice, communicating concerns to the Director, PI, study sponsor or IRB as needed.
• Notifies appropriate management and external parties of serious adverse events according to protocol.
• Maintains the study file record according to GCP.
• Maintains subject participant records according to GCP.
• Completes the clinical trials management system and electronic/paper case report forms in an accurate and timely manner
• Other duties as assigned.
• The position requires 20 – 25% travel between assigned facilities and various locations within the community.
EDUCATION:
• Bachelor’s Degree in Sciences or Technology required. Master’s degree is desired
o Clinical research experience, if possible, with Clinical Trials and clinical research training also preferred
Familiar with GCP and IRB regulations rules.
Ability to work independently and with other teams
About ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
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