Data Research Analyst – TX Center Joint Replacement– Full-Time, Days

#REF!•Plano, TX

12d•Onsite

About The Position

Here’s What You Need High School Diploma (REQUIRED) Bachelor's Degree bachelor's in biology or chemistry (REQUIRED) Master's Degree in biology or chemistry (PREFERRED) Two years of Clinical Research experience with a strong understanding of specified functional area (REQUIRED) CRC - Certified Clinical Research Coordinator with 18 months (REQUIRED) Demonstrates ability to produce publication-ready manuscripts and technical reports (STRONGLY PREFERRED) Familiar with the end-to-end editorial and submission process for publications (STRONGLY PREFERRED) What You Will Do: Participates in or leads the review of clinical documents (e.g., protocols, reports, data management and statistical analysis plans) by interacting with various groups. Plans and designs source documents for study protocols as required. Leads data collection and management activities, drafting Data Management Plans and Data Review Plans as required. Ensures adverse events (AE) are identified and reported per protocol compliance and the archiving of study databases and related documents by following established guidelines Leads the development of data management reports of clinical data. Leads the preparation and presentation of data management activities by evaluating and testing new systems. Leads Clinical Data Management activities by using Clinical knowledge, data listings and manual review of eCRFs to issue queries and clean data as required. Contributes to the monitoring of data quality during study conduct. Provides information on issues along with proposed solutions Responsible for implementing and maintaining the effectiveness of the quality system. Ensures data snapshots are ready for analysis by following established guidelines. Participates in the design, administration and monitoring of clinical trials. Updates and reviews regulatory documents. Performs other duties as assigned. . Additional perks of being a Texas Health employee Benefits include 401k, PTO, medical, dental, Paid Parental Leave, flex spending, tuition reimbursement, Student Loan Repayment Program as well as several other benefits. Delivery of high quality of patient care through nursing education, nursing research and innovations in nursing practice. Strong Unit Based Council (UBC). A supportive, team environment with outstanding opportunities for growth. Learn more about our culture, benefits, and recent awards. Entity Highlights: Texas Health Physicians Group includes more than 1,000 physicians, nurse practitioners and physician assistants dedicated to providing quality, patient-safe care at more than 240 offices located throughout the DFW Metroplex. THPG members are active in group governance and serve on multiple committees and councils. Ongoing Texas Health initiatives, like the Diversity Action Council and Living the Promise, have helped to create an inclusive, supportive, people-first, excellence-driven culture and workplace, making THPG a great place to work. If you’re ready to join us in our mission to improve the health of our community, then let’s show the world how we’re even better together! Do you still have questions or concerns? Feel free to email your questions to [email protected] . #LI-RE1 Data Research Analyst Bring your passion to Texas Health so we are Better + Together Work location \: 6020 West Parker Road - Suite 470 Plano, TX 75093 Work hours \: Full-time, 40 hours weekly, Monday thru Friday (830am-5pm) Digestive Specialists Clinic Highlights : Strong teamwork and collaboration Fast-paced Compassion and empathy to our patients and the Team Recognized in local publications

Requirements

High School Diploma (REQUIRED)
Bachelor's Degree bachelor's in biology or chemistry (REQUIRED)
Two years of Clinical Research experience with a strong understanding of specified functional area (REQUIRED)
CRC - Certified Clinical Research Coordinator with 18 months (REQUIRED)

Nice To Haves

Master's Degree in biology or chemistry (PREFERRED)
Demonstrates ability to produce publication-ready manuscripts and technical reports (STRONGLY PREFERRED)
Familiar with the end-to-end editorial and submission process for publications (STRONGLY PREFERRED)

Responsibilities

Participates in or leads the review of clinical documents (e.g., protocols, reports, data management and statistical analysis plans) by interacting with various groups.
Plans and designs source documents for study protocols as required.
Leads data collection and management activities, drafting Data Management Plans and Data Review Plans as required.
Ensures adverse events (AE) are identified and reported per protocol compliance and the archiving of study databases and related documents by following established guidelines
Leads the development of data management reports of clinical data.
Leads the preparation and presentation of data management activities by evaluating and testing new systems.
Leads Clinical Data Management activities by using Clinical knowledge, data listings and manual review of eCRFs to issue queries and clean data as required.
Contributes to the monitoring of data quality during study conduct.
Provides information on issues along with proposed solutions
Responsible for implementing and maintaining the effectiveness of the quality system.
Ensures data snapshots are ready for analysis by following established guidelines.
Participates in the design, administration and monitoring of clinical trials.
Updates and reviews regulatory documents.
Performs other duties as assigned.