Posted in Other 30+ days ago.
Type: Full Time
DESCRIPTION SHIFT: No Weekends
SCHEDULE: Full-time
SARAH CANNON is the research arm of HCA's global cancer enterprise. Focused on advancing therapies for patients, it is one of the world's leading clinical research organizations conducting community-based clinical trials in oncology, cardiology and orthopedics through affiliations with a network of more than 1,000 physicians across the United States and United Kingdom.
We believe our success is dependent on a healthy work environment where staff members are the core of advancing therapies for patients and accelerating drug development. We apply the same compassion and commitment we have for our patients to our co-workers and colleagues and promote an entrepreneurial culture.
BENEFITS:
* Tuition Reimbursement/Assistance Programs
* Paid Personal Leave
* 401k (100% annual match - 3%-9% of pay based on years of service)
* Identity Theft Protection discounts
* Auto, Home, and Life Insurance options
* Adoption Assistance
* Employee Stock Purchase Program (ESPP)
The MANAGER OF TISSUE OPERATIONS is responsible for overall tissue operations to support the institution's growing molecular profiling initiative, including direct supervision and development of staff, adherence to standard operating procedures and reporting of data to internal and external groups
* You will manage performance and professional development of the tissue operations staff.
* You will create, monitor, document and follow departmental SOPs, WPGs and corporate guidelines.
* You will ensure timely and accurate entry of molecular profiling data into assigned database, including transcription of pathology reports and review and documentation of patient history, prior therapies, current therapy status and routine therapy follow-up.
* You will ensure timely and accurate molecular profiling tissue collection process, including tissue requests, queries, tracking logs and shipments.
* You will prepare reports for leadership, sponsors, CROs and other individuals/groups as needed.
* You will meet with investigators, study monitors, and others in coordinating study logistics; participate in staff meetings, site initiation and other meetings which will impact the delivery of quality research and compliance.
* You will receive and triage information requests; research and provide information where appropriate.
* You will maintain positive and cooperative relationships in day-to-day interactions and communications.
* You will communicate and escalate unresolved issues at the appropriate time and to the appropriate level of management.
QUALIFICATIONS YOU SHOULD HAVE FOR THIS POSITION:
* A Bachelor Degree
* The ability to read, understand, and comply with research protocols.
* Strong computer skills with demonstrated ability using clinical trial databases, electronic data capture, MS Access or Excel
* Resourceful with heightened analytical abilities and problem solving skills in a fast paced environment.
* Excellent interpersonal skills, detailed-oriented and meticulous.
* Clinical and/or scientific experience in a research setting required
* Management experience required
* Clinical and/or Scientific experience in a research setting specifically with working with profiling preferred
* Research certification (ACRP or CCRP) preferred
DO YOU WANT TO WORK ON A TEAM FIGHTING CANCER TOGETHER? APPLY NOW TO LEARN MORE ABOUT THIS OPPORTUNITY.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
NOTICE
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