Actalent
Oncology Clinical Research Coordinator
Actalent, Houston, Texas, United States, 77246
Oncology Clinical Research Coordinator (Contract Position)
Job Description:
We are seeking a full time onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Oncology clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study. As the position and study progress, additional responsibilities may be assigned. The candidate must be flexible and willing to assist with various tasks as needed.
Key Responsibilities:
Participant Screening: Perform phone screenings or prescreen participants for eligibility.
Medical Record Review: Conduct thorough reviews of patient medical records.
Informed Consent: Obtain informed consent from trial participants.
Data Management: Collect study data and enter it into electronic data capture (EDC) systems.
Query Resolution: Address and resolve data queries promptly.
Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders.
Community Outreach: Networking with referral physicians, visiting clinics and hospitals to educate medical professionals and patients about the clinical trial, distributing study materials, posting recruitment materials, and maintaining online portals to track metrics.
General Support: Assist with any other study-related efforts as deemed necessary by the site.
Qualifications:
Minimum of three years of experience as a Clinical Research Coordinator
Experience in Oncology clinical trials required
Proficiency with electronic medical records (EMR)
Proficiency with CRIO electronic data capture (EDC) system preferred OR other EDC systems
Additional Details:
Location: Houston, TX - zip code 77079
Duration: Open ended contract - expected to be 6 months
Schedule: 30 hours per week (Monday-Friday) - during normal business hours
Hourly Pay Range: $25-35 per hour
Start Date: ASAP
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:
We are seeking a full time onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Oncology clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study. As the position and study progress, additional responsibilities may be assigned. The candidate must be flexible and willing to assist with various tasks as needed.
Key Responsibilities:
Participant Screening: Perform phone screenings or prescreen participants for eligibility.
Medical Record Review: Conduct thorough reviews of patient medical records.
Informed Consent: Obtain informed consent from trial participants.
Data Management: Collect study data and enter it into electronic data capture (EDC) systems.
Query Resolution: Address and resolve data queries promptly.
Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders.
Community Outreach: Networking with referral physicians, visiting clinics and hospitals to educate medical professionals and patients about the clinical trial, distributing study materials, posting recruitment materials, and maintaining online portals to track metrics.
General Support: Assist with any other study-related efforts as deemed necessary by the site.
Qualifications:
Minimum of three years of experience as a Clinical Research Coordinator
Experience in Oncology clinical trials required
Proficiency with electronic medical records (EMR)
Proficiency with CRIO electronic data capture (EDC) system preferred OR other EDC systems
Additional Details:
Location: Houston, TX - zip code 77079
Duration: Open ended contract - expected to be 6 months
Schedule: 30 hours per week (Monday-Friday) - during normal business hours
Hourly Pay Range: $25-35 per hour
Start Date: ASAP
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.