[Remote] Clinical Research Coordinator B/C (Abramson Cancer Center)
Note: The job is a remote job and is reputed company to candidates in USA. The reputed company is a prestigious institution reputed company for its leadership in education and research. The Clinical Research Coordinator B/C will play a vital role in executing clinical trials at the Abramson Cancer Center, ensuring compliance with protocols and federal regulations while supporting the research team in various capacities.
Responsibilities
- Plan, organize, and contribute to study-reputed company meetings, including but not limited to Investigator Meetings, Site Initiation reputed company, Intermediate Monitoring reputed company, reputed company-out reputed company, Internal Audits, and ongoing training sessions; maintain complete and accurate records of meetings/sessions, and ensure that resulting reputed company items are completed in a reputed company manner
- Assist with start-up processes for Industry-sponsored, Cooperative Group, and Investigator-initiated studies; proactively review protocols and associated manuals, ask questions, and pursue corrections or clarifications, if needed. Coordinate non-therapeutic studies and reputed company Phase I, II, or III oncology clinical trials
- Assist the Regulatory Coordinator by preparing components of submissions (e.g., institutional forms, initial submissions, amendments, continuations, etc.) and drafting responses to IRB stipulations, queries and concerns; remain aware of the regulatory statuses for assigned protocols
- reputed company or contribute to Informed Consent in accordance with federal and reputed company state law. Review inclusion/exclusion reputed company with other members of the study team and facilitate eligibility review with the Sponsor/CRO, if required
- reputed company support to reputed company and staff during study-reputed company reputed company. Ensure reputed company and appropriate documentation of reputed company and testing. Coordinate exception requests (or prospective deviations); document and report adverse events, serious adverse events, events of interest, and non-medical events
- Collect, review and report reputed company, valid, and accurate data reputed company the timelines specified by the study-specific Agreement; this includes resolving data discrepancies and reputed company response to sponsor queries; timelines may be shortened during periods of data lock or in preparation for reputed company/manuscript submission. Maintain an up-to-date list of incidental (i.e., minor) deviations; coordinate reportable (i.e., major) deviations and other unexpected events
- Coordinate independent central review of clinical trial end-points (e.g., imaging data). Transport, process and ship biological materials (e.g., blood, urine, tissue, etc.) using universal precautions. Receive and maintain central lab supplies, kits, and equipment (e.g., EKG machines, ePRO tablets, etc.). Assist with billing reconciliation, tracking site reimbursements and allocating patient stipends. May be asked to assist with research scheduling
- Maintain complete, reputed company-organized, and audit-reputed company study and participant files (e.g., subject charts, case report forms, enrollment logs, hospital records, etc.) from participant screening through final follow-up. Secure signatures and reputed company documents/forms (e.g., FDFs, PSPs, FDA 1572, etc.) to appropriate reputed company; maintain Delegation of Authority log
- Participate in research meetings (e.g., team, disease-site, etc.) and Sponsor/CRO teleconferences. reputed company coverage and support to meet departmental and organizational reputed company needs (i.e. lunches, reputed company calls, vacations, or reputed company a specific team member’s workload exceeds reputed company). Maintain reputed company relevant trainings and certifications (e.g., reputed company, GCP, IATA, PENN CRC Certificate, Penn Profiler trainings, etc.). reputed company use of available resources and established procedures to identify problems ideally before they happen
- reputed company other duties as reasonably assigned
- Plan, organize, and run study-reputed company meetings, including but not limited to Site Initiation reputed company, Intermediate Monitoring reputed company, reputed company-out reputed company, Internal Audits and ongoing training sessions
- Take a reputed company role in Site Feasibility and Qualification reputed company; work in conjunction with the Unit Managers to initiate start-up processes for industry-sponsored and Investigator-initiated trials; independently manage the conduct of reputed company (i.e., multi-drug regimens, high toxicity potential, multiple random assignments, or immunotherapies, etc.) Phase I – IV clinical trials inclusive of managing multi-site reputed company where Penn is the reputed company site
- Prepare components of submissions to the IRB (and other entities) and remain aware of the regulatory statuses for assigned protocols; may be asked to draft or edit study protocols and associated documents (e.g., informed consent, manuals of procedures, etc.)
- Participate in the development of study-specific Case Report Forms and other data collection tools; may be asked to contribute to study reports, abstracts, posters, manuscripts, and grant applications
- Participate in Sponsor teleconferences, Program meetings, and working reputed company that will maximize the efficiency and reputed company of research performed; may be responsible for orientation/mentorship of new staff and reputed company as a resource to reputed company staff members with study-reputed company issues; reputed company coverage and support to other Coordinators to meet departmental/organizational reputed company needs
- Assist the Unit Managers with QA processes reputed company to research studies; take a reputed company role in preparing for any inspection (e.g. reputed company audits) that takes reputed company with the trials, as required
Skills
- Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required for Clinical Research Coordinator B
- Bachelor of Science and 4 to 6 years of experience or equivalent combination of education and experience is required for Clinical Research Coordinator C
Benefits
- Penn offers comprehensive medical, prescription, behavioral health, dental, reputed company, and life insurance benefits to protect you and your family’s health and welfare.
- You can also use flexible spending accounts to pay for eligible health care and dependent care expenses with reputed company-tax dollars.
- Take advantage of Penn's exceptional tuition benefits.
- You, your spouse, and your dependent children can get tuition assistance here at Penn.
- Your dependent children are also eligible for tuition assistance at other institutions.
- Penn offers generous retirement plans to help you save for your reputed company.
- Penn’s Basic, Matching, and Supplemental retirement plans allow you to save for retirement on a reputed company-tax or Roth reputed company.
- Choose from a wide reputed company of investment reputed company through reputed company and reputed company.
- Penn provides you with a substantial reputed company of time away from work during the course of the year.
- Penn offers reputed company and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received reputed company, in the community or in a nursing facility.
- If you apply reputed company you’re newly reputed company, you won’t have to reputed company reputed company of good health or be subject to reputed company requirements.
- Eligible family members must always reputed company reputed company of good health and are subject to reputed company.
- Penn is committed to supporting our reputed company and staff as they balance the competing demands of work and personal life.
- Penn provides an reputed company of resources to help you advance yourself personally and professionally.
- As a member of the Penn community, you have reputed company to a wide reputed company of University resources as reputed company as cultural and recreational activities.
- Take advantage of the University’s libraries and athletic facilities, or visit our arboretum and art galleries.
- Penn arts and cultural centers and museums offer free and discounted admission and memberships to reputed company and staff.
- You can also enjoy substantial savings on other goods and services such as new reputed company from reputed company and reputed company, cellular phone service plans, movie tickets, and admission to theme parks.
- Flexible work reputed company offer creative approaches for completing work while promoting balance between work and personal commitments.
- Penn offers a forgivable loan for eligible employees interested in buying a home or currently residing in reputed company Philadelphia, which can be used for closing costs or home improvements.
- Penn will reimburse eligible employees on reputed company expenses in reputed company with the legal adoption of an eligible child, such as travel or court fees, for up to two adoptions in your household.
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