Research Coordinator at US Digestive Health

Altoona, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

09 Sep, 26

Salary

0.0

Posted On

11 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research Coordination, Data Management, Phlebotomy, Patient Recruitment, Specimen Processing, Regulatory Documentation, EMR Systems, Microsoft Office, Good Clinical Practice, IATA Training, Quality Control, Case Report Forms

Industry

Medical Practices

Description

Description Under general supervision, the Clinical Research Coordinator provides assistance to the Research Department, including recruitment, managing data, and collecting, processing, and coordinating samples, specimens, and information. DUTIES AND RESPONSIBILITIES: Provide assistance to Research staff by organizing files, projects, information and data. Collect, process, and assist in the compilation and verification of research data, samples, and/or specimens (following strict protocol and detailed instructions) Enter data from forms and documents into databases and other documents Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol Become familiar with Research SOPs and study protocols Ensure patient’s referring physician receives notification of patient’s participation in studies as requested by the patient Collect, process, and ship blood/urine/stool specimens at patient visits Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy Submit patient stipends/reimbursement requests at the conclusion of study visits Ensure the filing and maintenance of all regulatory documents Maintain temperature logs Order and distribute dry ice as needed Periodically check expiration dates on clinical supplies and re-order as needed Assist coordinators with preparation of source documents Assist with subject recruitment by performing chart reviews, cold calling, etc. Schedule patient visits Process Lab specimens Assist with vital signs Perform Fibroscans once trained Phlebotomy Provide general office support to keep operations running smoothly Other duties as assigned QUALIFICATIONS & REQUIREMENTS: Able to effectively present information and respond to questions from physicians, staff and patients Proficiency in Microsoft Office software preferred, knowledge of EMR systems required Able to function effectively in a team setting Must have critical thinking skills Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals Able to demonstrate consistent professional conduct and meticulous attention to detail Completion of Good Clinical Practice and IATA training required Must be able to work flexible hours as necessary Previous phlebotomy experience preferred Must be a self-starter and demonstrate initiative Willingness to learn is a must Schedule Type: Day shift, Monday to Friday, No weekends Requirements Completion of bachelor’s degree (in lieu of degree four years of relevant clinical research experience may be accepted) Minimum two years of experience in a related healthcare position Previous experience with clinical trials a must Experience with pharmaceutical trials preferred

Responsibilities

The Clinical Research Coordinator assists the Research Department with patient recruitment, data management, and the collection and processing of biological specimens. They are responsible for maintaining regulatory documents, ensuring data integrity, and coordinating study visits according to strict protocols.