Stanford University
Clinical Research Coordinator Associate (Hybrid Opportunity)
Stanford University, Stanford, California, United States, 94305
Clinical Research Coordinator Associate (Hybrid Opportunity)
The Division of Pulmonary, Allergy and Critical Care Medicine (PACCM) is seeking a Clinical Research Coordinator Associate (CRCA) to join their expanding clinical research program. This is an opportunity to work in an intellectually stimulating and collaborative research environment focused on the care of patients with lung diseases from a variety of causes. This CRCA will perform duties related to the coordination of moderately complex aspects of multiple pulmonary research protocols, including industry-sponsored, NIH and PI-initiated investigational drug clinical trials as well as blood and tissue banking registries. This position has a focus in Non-Tuberculous Mycobacterial (NTM) Lung Disease, Idiopathic Pulmonary Fibrosis (IPF), and Progressive Pulmonary Fibrosis (PPF), but may involve other lung disease study areas. Excellent computer skills are required including MS Word, Power Point, and Excel. The candidate must also demonstrate strong written and verbal communication skills and the ability to take initiative and work as a team player or independently. Duties include: Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study specimens and processing. Collect and manage patient and laboratory data for clinical research projects. Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors. Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff. Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct. DESIRED QUALIFICATIONS: Experience with interventional drug treatment trials. Clinical experience with patients with pulmonary disease. Completion of a clinical trials certification program or related courses. EDUCATION & EXPERIENCE (REQUIRED): Two-year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience. KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED): Strong interpersonal skills. Proficiency with Microsoft Office. Knowledge of medical terminology. Stanford University is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.
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The Division of Pulmonary, Allergy and Critical Care Medicine (PACCM) is seeking a Clinical Research Coordinator Associate (CRCA) to join their expanding clinical research program. This is an opportunity to work in an intellectually stimulating and collaborative research environment focused on the care of patients with lung diseases from a variety of causes. This CRCA will perform duties related to the coordination of moderately complex aspects of multiple pulmonary research protocols, including industry-sponsored, NIH and PI-initiated investigational drug clinical trials as well as blood and tissue banking registries. This position has a focus in Non-Tuberculous Mycobacterial (NTM) Lung Disease, Idiopathic Pulmonary Fibrosis (IPF), and Progressive Pulmonary Fibrosis (PPF), but may involve other lung disease study areas. Excellent computer skills are required including MS Word, Power Point, and Excel. The candidate must also demonstrate strong written and verbal communication skills and the ability to take initiative and work as a team player or independently. Duties include: Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study specimens and processing. Collect and manage patient and laboratory data for clinical research projects. Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors. Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff. Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct. DESIRED QUALIFICATIONS: Experience with interventional drug treatment trials. Clinical experience with patients with pulmonary disease. Completion of a clinical trials certification program or related courses. EDUCATION & EXPERIENCE (REQUIRED): Two-year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience. KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED): Strong interpersonal skills. Proficiency with Microsoft Office. Knowledge of medical terminology. Stanford University is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.
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