Clinical Research Coordinator II
3 weeks ago
Stanford University has partnered with iHire to reach top talent for their opening below. Check it out and apply via iHireBiotechnology today The Department of Neurology at Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively more complex projects/assignments. Independently manage significant and key aspects of a large study or all aspects of one or more small research studies. Duties include: Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. Oversee data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data. Develop project schedules, targets, measurements, and accountabilities, as assigned. Lead team meetings and prepare/approve minutes. Formally supervise, train, and/or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work. Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to requests and questions. Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries. Provide leadership in determining, recommending, and implementing improvements to policies/processes; define best practices. Develop study budget with staff and principal investigator, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract. Ensure regulatory compliance. Regularly inspect study documents to ensure ongoing regulatory compliance. Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed. Other duties may also be assigned. Education & Experience (required) Bachelor's degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience. Knowledge, Skills and Abilities (required) Strong interpersonal skills. Proficiency with Microsoft Office and database applications. Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. Knowledge of medical terminology. Certifications & Licenses Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. PHYSICAL REQUIREMENTS* Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping. Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds. Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more. Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job. Working Conditions Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections. May require extended or unusual work hours based on research requirements and business needs. Work Standards Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations. Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned. Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide. The expected pay range for this position is $86,248 to $100,158 per annum. Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs. At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website provides detailed information on Stanford’s extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process. Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a contact form. Stanford 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. The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned. #J-18808-Ljbffr
-
Clinical Research Coordinator
3 weeks ago
Sunnyvale, United States Actalent Full timeClinical Research Coordinator (Oncology) Job Title: Clinical Research Coordinator We are seeking a dedicated Clinical Research Coordinator to serve as the primary contact for research participants, sponsors, and regulatory agencies. This role involves coordinating studies from startup through close‑out and ensuring the smooth operation of clinical trials....
-
Clinical Research Coordinator
3 weeks ago
Sunnyvale, United States Actalent Full timeJob Title: Clinical Research Coordinator Job Description We are seeking a dedicated Clinical Research Coordinator to serve as the primary contact for research participants, sponsors, and regulatory agencies. This role involves coordinating studies from startup through close-out and ensuring the smooth operation of clinical trials. Responsibilities Act as the...
-
Oncology Clinical Research Coordinator
3 weeks ago
Sunnyvale, United States Actalent Full timeA leading clinical research organization is seeking a Clinical Research Coordinator to manage clinical trials from startup to close-out. The role involves direct contact with research participants, sponsors, and regulatory bodies, ensuring compliance with protocols. Candidates should have at least 2 years of coordination experience and familiarity with...
-
Sunnyvale, United States Actalent Full timeA global leader in engineering and sciences services is seeking a Clinical Research Coordinator to facilitate clinical trials. You will manage study coordination, interact with participants, and ensure compliance with protocols. Ideal candidates will have at least 2 years of experience and familiarity with oncology trials. The position offers a hybrid work...
-
Space Mission Analyst
6 days ago
Sunnyvale, United States Lockheed Martin Full timeJob share URL Featured Job Allows Referral Featured Job Allows Referral Space Mission Analyst / Operations Research II | Lockheed Martin
-
Senior Clinical Research Associate
1 week ago
Sunnyvale, United States CYNET SYSTEMS Full timeJob Description: Pay Range: $79.93hr - $89.93hr The Senior Clinical Research Associate (CRA) will contribute to the start-up, execution, and management of clinical studies from initiation through FDA approval. This role involves collaboration with internal teams, clinical sites, and external partners to ensure study compliance, accuracy, and efficiency in...
-
Clinical Research Associate
1 week ago
Sunnyvale, CA, United States Experis Full timeTitle: Clinical Research Associate (CRA) Location: Sunnyvale, CA Duration: 12 Months Pay Range: $45 to $50/hr We are looking for an Internal Clinical Research Associate (CRA) to join one of our growing Clinical Operations teams. Job Summary: The Internal CRA will assist in managing clinical research sites throughout the entire trial lifecycle-from start-up...
-
Clinical Research Associate
2 weeks ago
Sunnyvale, CA, United States Experis Full timeTitle: Clinical Research Associate (CRA) Location: Sunnyvale, CA Duration: 12 Months Pay Range: $45 to $50/hr We are looking for an Internal Clinical Research Associate (CRA) to join one of our growing Clinical Operations teams. Job Summary: The Internal CRA will assist in managing clinical research sites throughout the entire trial lifecycle-from start-up...
-
Clinical Research Associate
1 week ago
Sunnyvale, CA, United States Experis Full timeTitle: Clinical Research Associate (CRA) Location: Sunnyvale, CA Duration: 12 Months Pay Range: $45 to $50/hr We are looking for an Internal Clinical Research Associate (CRA) to join one of our growing Clinical Operations teams. Job Summary: The Internal CRA will assist in managing clinical research sites throughout the entire trial lifecycle-from start-up...
-
Clinical Research Associate
3 days ago
Sunnyvale, CA, United States Experis Full timeTitle: Clinical Research Associate (CRA) Location: Sunnyvale, CA Duration: 12 Months Pay Range: $45 to $50/hr We are looking for an Internal Clinical Research Associate (CRA) to join one of our growing Clinical Operations teams. Job Summary: The Internal CRA will assist in managing clinical research sites throughout the entire trial lifecycle-from start-up...