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Clinical Research Coordinator I - Hematology
Location:
Philadelphia, PA
Description:
SHIFT:Day (United States of America) Seeking Breakthrough Makers Children's Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation.At CHOP, your experience is valued; your voice is heard; and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care-and your career. CHOP's Commitment to Diversity, Equity, and Inclusion CHOP is committed to building an inclusive culture where employees feel a sense of belonging, connection, and community within their workplace. We are a team dedicated to fostering an environment that allows for all to be their authentic selves. We are focused on attracting, cultivating, and retaining diverse talent who can help us deliver on our mission to be a world leader in the advancement of healthcare for children.We strongly encourage all candidates of diverse backgrounds and lived experiences to apply. A Brief Overview The Children's Hospital of Philadelphia, Division of Hematology, is hiring a full-time clinical research coordinator.The research coordinator will work on clinical studies involving pyruvate kinase deficiency, thalassemia, sickle cell disease, and gene therapy. Specific research projects will be discussed at the time of interview.Opportunities are available to attend weekly Hematology Divisional Clinical Conference and weekly Department of Pediatrics Grand Rounds, which provide unique insight into a large tertiary pediatric hospital. Research staff are required to attend disease program weekly clinical meetings.This position involves regular interaction with patients in a clinical setting and the opportunity to build relationships with patients and their families. It may also include travel to hematology conferences (depending on COVID precautions in place), authorship and publishing opportunities.Job Description:Research-related: Act as study coordinator and primary contact for several multi-center clinical research activities and possibly CHOP investigator-led studies. Within the scope of clinical research protocols, participate in direct patient care. Assist with budget and contract preparations. Prepare consent documents, screen and track eligible patients, obtain and maintain Institutional Review Board (IRB) approvals. Coordinate sponsor monitoring visits. Carry out day-to-day requirements of clinical research projects including coordinating study visits, interviewing patients, data collection, data entry, response to queries, and budgetary matters.Facilitate the conduct of clinical research within the CHOP healthcare network. Serve as an information conduit between Research Administration and investigators, sharing information and collecting and submitting materials as requested. Provide broad support for investigators in carrying out the administrative aspects of their research programs.Program Related: Assist with center projects including (but not limited to) trainee and family educational and resource materials, patient satisfaction surveys, center-sponsored patient and family activities, professional academic presentations of physicians, nurses and social workers, and other projects as needed. Assist with grant preparations. Requirements: Graduate of an accredited college with a minimum of a Bachelor's Degree in a health related field, or with related healthcare experience or interest. Prior research experience, particularly regulatory experience, is required; must demonstrate an interest in research. Facility with Microsoft Office Suite and database management. Successful performance in a high-intensity work environment and ability to handle multiple tasks simultaneously. Excellent problem identification and problem-solving skills required. Must also be independent, efficient and possess exceptional interpersonal skills, as interaction with patients, families, and medical staff is frequent. Flexibility is essential. What you will do Core responsibilities Adhere to an IRB approved protocol Participate in the informed consent process of study subjects Support the safety of clinical research patients/research participants Coordinate protocol related research procedures, study visits, and follow-up care Screen, recruit and enroll patients/research participants Maintain study source documents Under the supervision of PI Report adverse events Understand good clinical practice (GCP) and regulatory compliance Educate subjects and family on protocol, study intervention, etc. Comply with Institutional policies, standard operating procedures (SOPs) and guidelines, and with HIPAA and management of confidential materials Must comply with federal, state, and sponsor policies For multi-site studies or collaborations, support communication and meeting scheduling across teams Related responsibilities Manage essential regulatory documents Register study on ClinicalTrials.gov as appropriate Complete case report forms (paper & electronic data capture) and address queries Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie,DSMB, independent safety officer) Facilitate pre-study, site qualification, study initiation, and monitoring visit as appropriate Facilitate study close out activities as appropriate Coordinate research/project team meetings Collect, process and ship samples as applicable to the protocol Schedule subject visits and procedures Retain records/archive documents after study close out Education Qualifications High School Diploma / GED Required Bachelor's Degree Preferred Experience Qualifications At least two (2) years of clinical or clinical related or research related experience Required At least three (3) years of clinical or clinical related or research related experience Preferred Skills and Abilities Basic knowledge of IRB and human subject protection Strong verbal and written communications skills Strong time management skills Ability to collaborate with stakeholders at all levels To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must be fully vaccinated against COVID-19 and receive an annual influenza vaccine. Learn more. Employees may request exemptions for valid religious and medical reasons. Start dates may be delayed until candidates are immunized or exemption requests are reviewed. EEO / VEVRAA Federal Contractor | Tobacco Statement
Company:
Children's Hospital Of Philadelphia
Industry:
Other
Posted:
May 17 on Professional Diversity Network
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More About this Listing: Clinical Research Coordinator I - Hematology
Clinical Research Coordinator I - Hematology is a Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Job at Children's Hospital of Philadelphia located in Philadelphia PA. Find other listings like Clinical Research Coordinator I - Hematology by searching Oodle for Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Jobs.
Clinical Research Coordinator I - Hematology is a Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Job at Children's Hospital of Philadelphia located in Philadelphia PA. Find other listings like Clinical Research Coordinator I - Hematology by searching Oodle for Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Jobs.