Clinical Research Associate for Memory Disorders
About The Position
The Clinical Research Associate serves as project lead for the execution of existing lymphoproliferative disorder studies. The role oversees study milestones, troubleshoots issues, and collaborates with the physician lead, physician extenders, research staff, and industry or academic sponsors. It also establishes an IRB-approved registry to track patients participating in clinical trials and research initiatives. The associate co-authors manuscripts for peer-reviewed scientific journals, assists in developing concepts into protocols, and supports manuscript preparation and abstract presentations for national and international meetings based on current initiatives and clinical trial findings. The position collaborates on protocols to implement best practices and develops an educational outreach platform with local healthcare providers and community organizations to raise awareness of research initiatives and clinical trial opportunities. The role participates in tumor boards, relevant conferences, and research and service line meetings as directed by the physician lead. It also collaborates with the CRC assigned to the protocols to assist with data entry for the tissue registry.
Requirements
- Bachelor's degree in a related science.
- Experience conducting research in a clinical or pre-clinical setting.
Responsibilities
- Lead execution of existing lymphoproliferative disorder studies, including meeting milestones, troubleshooting, and coordinating with the physician lead, physician extenders, research staff, and trial sponsors.
- Establish an IRB-approved registry to track patients participating in clinical trials and research initiatives.
- Co-author manuscripts for submission to peer-reviewed scientific journals.
- Assist in developing concepts into protocols and collaborate on protocols to implement best practices.
- Support manuscript preparation and abstract presentations for national and international meetings based on current initiatives and clinical trial findings.
- Create an educational outreach platform with local healthcare providers and community organizations to raise awareness about research initiatives and clinical trial opportunities.
- Participate in tumor boards, relevant conferences, and research and service line meetings as directed by the physician lead.
- Collaborate with the CRC assigned to the protocols to assist with data entry for the tissue registry.
Benefits
- Health benefits
- Life insurance
- Long-term disability coverage
- Healthcare spending accounts
- Retirement plan
- Paid time off
- Pet insurance
- Tuition reimbursement
- Employee assistance program
- Wellness program
- On-site housing for select positions
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
