Clinical Research Specialist (Neurology Department)

Houstonmethodistcareers; Houston (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Houston Methodist is seeking a Clinical Research Specialist to support multiple projects under supervision of the Clinical Trial Manager. Responsibilities include collecting patient data, following study protocols, and maintaining accurate documentation to ensure participant safety.

The role emphasizes teamwork with investigators, nurses, and coordinators, plus communication with patients and staff. You will assist with data reports and perform basic data analysis while ensuring compliance with

Qualifications

• Bachelor’s degree in a related field required.
• Bachelor's in health-science related field preferred.
• One year healthcare setting experience preferred.

Responsibilities

• Supports inter-professional team of clinical research investigators, nurses and coordinators.
• Performs data collection, abstraction and recording in CRFs.
• Makes phone calls to study patients for appointment reminders and follow-up.
• Transports and processes lab samples per the study manual of operations.

Skills

English proficiency

Communication skills

Listening skills

Independent work

Problem solving

Time management

Customer service

Critical thinking

Education

Bachelor’s degree in a related field

Bachelor's Degree in a Health-Science related field preferred

Job description

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.

FLSA STATUS

Exempt

QUALIFICATIONS

EDUCATION

• Bachelor’s degree in a related field
• Bachelor's Degree in a Health-Science related field preferred

EXPERIENCE

• One year experience in healthcare setting preferred
• Research setting preferred

SKILLS AND ABILITIES

• 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

ESSENTIAL FUNCTIONS

PEOPLE ESSENTIAL FUNCTIONS

• 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.
• 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 workflow 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.

SUPPLEMENTAL REQUIREMENTS

WORK ATTIRE

• Uniform: No
• Scrubs: Yes
• Business professional: Yes
• Other (department approved): No

ON-CALL*

*Note that employees may be required to be on-call during emergencies (ie. Disaster, Severe Weather Events, etc) regardless of selection below.

• On Call* No

TRAVEL**

**Travel specifications may vary by department**

• May require travel within the Houston Metropolitan area Yes
• May require travel outside Houston Metropolitan area No