- Supports the inter-professional team of clinical research investigators, nurses and coordinators. Promotes a positive work environment and contributes to a dynamic, team-focused work unit that actively helps one other to achieve optimal department results.
- Conducts self in a manner that is congruent with cultural diversity, equity and inclusion principles. Contributes towards improvement of department scores for employee engagement, i.e. peer-to-peer accountability SERVICE ESSENTIAL FUNCTIONS
- Performs clinical research support functions as assigned by the clinical trial manager including but not limited to informed consent for non-interventional studies, data abstraction and recording in CRFs
- Makes phone calls to study patients for appointment reminders and follow-up
- Transports blood and tissue samples. Processes and packages lab samples for shipping to sponsor or storage at site per the study manual of operations. QUALITY/SAFETY ESSENTIAL FUNCTIONS
- Completes required case report forms and resolves queries. Ensures accurate data collection, documentation organization, and safety of study volunteers. Ensures accurate regulatory filing
- Assists Clinical Trial Manager in identifying opportunities research work flow process improvement, providing recommendations, and contributes to meeting department and hospital targets for quality and safety FINANCE ESSENTIAL FUNCTIONS
- Assures study conduct meets appropriate IRB, FDA, ICH and agency guidelines
- Utilizes resources with cost effectiveness and value creation in mind. Self-motivated to independently manage time effectively and prioritize daily tasks, assisting coworkers as needed GROWTH/INNOVATION ESSENTIAL FUNCTIONS
- Assist in simple data analysis, with development of training materials for data reports, systems and collection and report generation
- Leads and identifies opportunities for performance improvement. Supports change initiatives and adapts to unexpected changes
- Seeks opportunities to identify self-development needs and takes appropriate action. Ensures own career discussions occur with appropriate management. Completes and updates the My Development Plan on an on-going basis This job description is not intended to be all-inclusive; the employee will also perform other reasonably related business/job duties as assigned. Houston Methodist reserves the right to revise job duties and responsibilities as the need arises.
- Bachelor's degree in health science-related field WORK EXPERIENCE
- One year experience in healthcare setting preferred
- Research setting preferred LICENSES AND CERTIFICATIONS - REQUIRED
- N/A
- Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going skills, competency assessments, and performance evaluations
- Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security
- Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles
- Exhibits good listening skills
- Ability to work independently and analyze and solve problems
- Demonstrates the ability to manage clinical and interpersonal situations
- Able to prioritize tasks and manage multiple projects
- Self-motivated with the ability to think critically and work independently
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Clinical Research Specialist - Houston, United States - Houston Methodist
Description
Clinical Research Specialist - Transplant - Admin
REFER A FRIEND Current Employees Apply BACK Location: Houston Methodist Academic Institute6670 Bertner Ave
Houston, TX 77030
Job Ref: 55455 Talent Area: Academic Institute Job Shift: 1st - Day Job Type: Full-Time Posted Date: April 29, 2024
At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols, gathering patient data via methods specified in the study protocol, study reports. This position ensures accurate data collection, documentation organization, and safety of study volunteers.
Requirements:
PEOPLE ESSENTIAL FUNCTIONSQualifications:
EDUCATION KNOWLEDGE, SKILLS, AND ABILITIES
