Clinical Research Manager
Website Retina Consultants of Houston
Retina Consultants of Houston
Company : Retina Consultants of Houston
Country: United States
Location : Conroe, Texas
Post: Thu, 09 Sep 2021 16:01:48 GMT
Expires: Thu, 07 Oct 2021 23:59:59 GMT
Apply Job : Apply Online
—————————— Job Description ——————————
The Clinical Research Manager will have experience in management of multi-center studies/clinical trials and strong interpersonal, communication, and project management skills, as well as be comfortable interacting with individuals at all levels of clinical research – from research assistants and Principal Investigators to patients enrolled in the study. The individual should be able to manage a large research team and provide them with guidance. This position ensures adherence to all applicable regulations, Good Clinical Practices, and industry standards governing research involving human subjects; and ensures that clinical studies are performed with the upmost integrity and quality.
RCTX offers the following competitive benefits for full-time elgible employees after the introductory period:
Medical Insurance Plans
Vision Insurance Plan
Dental Insurance Plan
PTO and Vacation Pay
Incentive Rewards Program
Retina Consultants of Texas (RCTX) is part of Retina Consultants of America (RCA), the largest network of leading retina specialists with the mission of saving sight and improving patient lives through innovation and the highest quality care. Through RCA’s physician-centered practice management model, physicians continue to drive clinical and practice culture while benefitting from the available business expertise, resources and shared best practices.
Retina Consultants of Texas is one of the largest and most respected retina-only ophthalmology practices in the United States, committed to Preserving the Patient’s Vision. RCTX has three certified research centers and is home to the Greater Houston Retina Research Center, one of the country’s leading sites for retinal research. All Retina Consultants of Texas physicians are board certified by the American Board of Ophthalmology and specialize exclusively in diseases and surgery of the retina, vitreous, and macula. In addition, RCTX has an ocular oncology division, which focuses on cancer treatments for the eye. Our surgeons have studied at some of the most renowned institutions in the nation and all have graduated at the very top of their classes.
Retina Consultants of Texas follows all CDC and local authority protocols to ensure the safety and well-being of the patients, providers, employees and communities.
Retina Consultants of Texas is proud to be an Equal Employment Opportunity and an Affirmative Action Employer. We are committed to creating an inclusive work environnment that celebrates diversity.
Staff management and proactive assessment of staffing needs to include hiring, training, and coaching/mentoring staff
Provide mentorship and guidance to team members and cross-functional staff on study processes and study requirements
Manage site workflow to ensure that patients/subjects, staff, and sponsors have the best customer service experience
Oversight of study management including timely review of monitor reports and associated study deliverables
Oversight of site study audits and inspections as needed
Identify, assess, and work with the QA team to resolve site performance and quality/compliance issues
Coordinate and manage various tasks in collaboration with the QA team & Regulatory Manager to achieve site readiness for timely first patient first visit
Obtain and maintain in-depth understanding of the study protocols and related procedures in order to contribute to the study team knowledge by sharing best practices, making recommendations for continuous improvement and providing training as needed/required
Ensure site meets monthly screening, randomization, and completion/retention goals by assessing scheduling, troubleshooting, and maximizing staff availability
Follow a quality process as outlined in the Site’s SOP’s to ensure the site collects and enters high quality data and to reduce preventable deviations
Ensure the site has high morale and works well as a team and meets our cultural goals and expectations
Bachelor’s Degree Required
5+ years of clinical research operations management-level experience
Knowledge, Skills, and Abilities:
Experience in people management and management best practices required
Excellent working knowledge of ICH GCP (International Conference on Harmonization, Good Clinical Practice) guidelines
Certified Clinical Research Professional (CCRP) certification preferred
Strong experience in clinical research is preferred
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