Medix™
This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $28.00/hr - $33.00/hr
Recruitment Advisor, Clinical Research & Life Sciences at Medix™ 6 month contract to full-time hire with company - paid weekly every Friday and benefits available after 30 days on contract.
Pay: $28-$33/hr based on years of experience and qualifications met
Mon-Fri 8-5 onsite
The client is looking for candidates with experience in:
2 + years of coordinating clinical trials as CRC or RA
Multiple therapeutic areas expertise, Oncology a Plus+ (you will be working within the client's Oncology team so comfortable working with Oncology patients as well)
Patient facing experience, no remote CRC work
The position requires a
Bachelor’s degree .
Key Responsibilities:
Serve as a primary point of contact for study participants, ensuring a positive and informed experience throughout their participation.
Assist with patient recruitment, screening, informed consent, and enrollment in oncology clinical trials.
Coordinate study visits, including scheduling, patient check-in, and preparation of required documentation.
Support research nurses and investigators during patient visits, including collection of vitals, specimen handling, and data recording (as permitted by scope and certification).
Communicate effectively with patients, families, and the clinical care team to facilitate adherence to study requirements.
Administrative & Research Support Duties:
Provide administrative support to the research nursing staff, including managing study binders, visit checklists, and data entry into electronic case report forms (eCRFs).
Maintain accurate and organized study documentation in compliance with Good Clinical Practice (GCP) and institutional SOPs.
Assist in preparing and submitting regulatory documents (IRB submissions, amendments, continuing reviews, etc.).
Track study supplies, ensure accurate specimen labeling/shipment, and manage inventory related to study conduct.
Coordinate communication between the clinical team, sponsors, and research office.
Participate in study meetings, site initiation visits, monitoring visits, and audits as needed.
Seniority level Mid-Senior level
Employment type Full-time
Job function Research and Health Care Provider
Industries Research Services and Hospitals and Health Care
Benefits
Medical insurance
Vision insurance
401(k)
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Base pay range $28.00/hr - $33.00/hr
Recruitment Advisor, Clinical Research & Life Sciences at Medix™ 6 month contract to full-time hire with company - paid weekly every Friday and benefits available after 30 days on contract.
Pay: $28-$33/hr based on years of experience and qualifications met
Mon-Fri 8-5 onsite
The client is looking for candidates with experience in:
2 + years of coordinating clinical trials as CRC or RA
Multiple therapeutic areas expertise, Oncology a Plus+ (you will be working within the client's Oncology team so comfortable working with Oncology patients as well)
Patient facing experience, no remote CRC work
The position requires a
Bachelor’s degree .
Key Responsibilities:
Serve as a primary point of contact for study participants, ensuring a positive and informed experience throughout their participation.
Assist with patient recruitment, screening, informed consent, and enrollment in oncology clinical trials.
Coordinate study visits, including scheduling, patient check-in, and preparation of required documentation.
Support research nurses and investigators during patient visits, including collection of vitals, specimen handling, and data recording (as permitted by scope and certification).
Communicate effectively with patients, families, and the clinical care team to facilitate adherence to study requirements.
Administrative & Research Support Duties:
Provide administrative support to the research nursing staff, including managing study binders, visit checklists, and data entry into electronic case report forms (eCRFs).
Maintain accurate and organized study documentation in compliance with Good Clinical Practice (GCP) and institutional SOPs.
Assist in preparing and submitting regulatory documents (IRB submissions, amendments, continuing reviews, etc.).
Track study supplies, ensure accurate specimen labeling/shipment, and manage inventory related to study conduct.
Coordinate communication between the clinical team, sponsors, and research office.
Participate in study meetings, site initiation visits, monitoring visits, and audits as needed.
Seniority level Mid-Senior level
Employment type Full-time
Job function Research and Health Care Provider
Industries Research Services and Hospitals and Health Care
Benefits
Medical insurance
Vision insurance
401(k)
#J-18808-Ljbffr