Overnight Clinical Trial Assistant
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Schedule
12-hour shift, no weekends 7:00 PM-7 :00 AM
Overnight Clinical Trial Assistant
Assist with informing patients of the protocol, screening patients, and assisting the research nurses; record the data and entering it in real time
Verify patient information by interviewing patient, recording medical history, and confirming purpose of
visit
Take blood pressure, weight, and temperature and collecting patient history summary
Perform blood draw and sample processing
Learn study protocols and introduce studies to patients accurately
Schedule patients based on the activity schedule in the study protocol
Help patients by providing information, services, and assistance
Maintain medical supplies inventory and perform preventive maintenance to keep medical equipment operational
Keep supplies ready by inventorying stock, placing orders, and verifying receipt
Communicate with the team, patients, and study sponsors appropriately and professionally
Maintains safe, secure, and healthy work environment by establishing and following standards and procedures and complying with legal regulations
Qualifications
Must have a minimum of 1 year of Medical Assistant or Clinical Research Assistant experience
Be trained or have experience in clinical research GCP requirements and medical documentation requirements
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:
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.
12-hour shift, no weekends 7:00 PM-7 :00 AM
Overnight Clinical Trial Assistant
Assist with informing patients of the protocol, screening patients, and assisting the research nurses; record the data and entering it in real time
Verify patient information by interviewing patient, recording medical history, and confirming purpose of
visit
Take blood pressure, weight, and temperature and collecting patient history summary
Perform blood draw and sample processing
Learn study protocols and introduce studies to patients accurately
Schedule patients based on the activity schedule in the study protocol
Help patients by providing information, services, and assistance
Maintain medical supplies inventory and perform preventive maintenance to keep medical equipment operational
Keep supplies ready by inventorying stock, placing orders, and verifying receipt
Communicate with the team, patients, and study sponsors appropriately and professionally
Maintains safe, secure, and healthy work environment by establishing and following standards and procedures and complying with legal regulations
Qualifications
Must have a minimum of 1 year of Medical Assistant or Clinical Research Assistant experience
Be trained or have experience in clinical research GCP requirements and medical documentation requirements
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
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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