Actalent
Clinical Research Coordinator II
Actalent, Kissimmee, Florida, United States, 34747
Job Title: Clinical Research Coordinator IIWork SiteThis is a fully on-site position in Orlando, Florida.
Job Description
As a Clinical Research Coordinator, you will be planning, coordinating, evaluating, and performing care of participants while collecting data for assigned research projects. Your work will involve close communication with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead and other clinical research support staff. Your primary responsibility will be to advocate for the patient while adhering to industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines. You will also act as a liaison between Principal Investigators, the Institutional Review Board (IRB), and the Office of Sponsored Programs (OSP). A key part of your role will involve preparing all documentation for clinical research and ensuring a timely turnaround of all documents to avoid delays in study initiation and/or progress. You will be expected to manage multiple clinical trial protocols, coordinate the execution and follow-up of each protocol, and manage records, study medication, and test articles in a confidential and secure manner.
Requirements:
2+ years experience as a Clinical Research Coordinator
Bilingual in English and Spanish
4 year degree within healthcare related field
Benefits:
Medical, Dental & Vision Plans
401k
Paid Holiday & Vacations
Employee Assistance Program
Corporate discounts and much more!
*Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for more information. *
About Actalent
Actalent 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 & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Job Description
As a Clinical Research Coordinator, you will be planning, coordinating, evaluating, and performing care of participants while collecting data for assigned research projects. Your work will involve close communication with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead and other clinical research support staff. Your primary responsibility will be to advocate for the patient while adhering to industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines. You will also act as a liaison between Principal Investigators, the Institutional Review Board (IRB), and the Office of Sponsored Programs (OSP). A key part of your role will involve preparing all documentation for clinical research and ensuring a timely turnaround of all documents to avoid delays in study initiation and/or progress. You will be expected to manage multiple clinical trial protocols, coordinate the execution and follow-up of each protocol, and manage records, study medication, and test articles in a confidential and secure manner.
Requirements:
2+ years experience as a Clinical Research Coordinator
Bilingual in English and Spanish
4 year degree within healthcare related field
Benefits:
Medical, Dental & Vision Plans
401k
Paid Holiday & Vacations
Employee Assistance Program
Corporate discounts and much more!
*Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for more information. *
About Actalent
Actalent 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 & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.