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Clinical Research Manager

  • Permanent
  • Anywhere

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 ——————————

Overview:
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

401K Contribution

Life Insurance

PTO and Vacation Pay

Incentive Rewards Program

Certification Opportunities

 

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. 

Responsibilities:
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

Qualifications:
Education Requirements

Bachelor’s Degree Required

 Experience Requirements:

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

To apply for this job please visit www.resume-library.com.