Job Details
Peachtree Dunwoody - Atlanta GA
Full Time
4 Year Degree
As needed for business requirements.
Ancillary Services
Description
GENERAL SUMMARY OF DUTIES : Responsible for assisting Primary Investigator with all clinical and organizational tasks for clinical research projects and protocols. Responsible for enrolling patients in protocols as per inclusion / exclusion criteria conducting follow-up visits drawing processing and shipping specimens entering study data reporting safety events and following all GCP guidelines. Responsible for all study coordinator protocol tasks assigned by Primary Investigator.
REPORTS TO : Primary Investigator and Research Manager
RESPONSIBILITIES
Duties include but are not limited to :
- Monitors protocols and organizes patient visits and tests
- Carries out duties and functions as directed by Primary Investigator and protocol
- Accurately maintains patient records to comply with demands and criteria of protocols amendments site visits conference calls and emergency adjustments
- Manages patient records to ensure clinical information is complete and filed appropriately in a timely systematic and tidy manner
- Has strong knowledge of protocols and goals
- Performs upkeep of exam and work rooms with regard to sterilization infection control supplies and equipment
- Observes strict infections disease precautions when handling blood specimens; wears a face mask and gloves
- Answers emails and voicemails and returns patient calls in a timely and efficient manner
- Completes requests for information from other UD staff and ensures that they are handled promptly and effectively to guarantee payment on patient accounts
- Maintains strict compliance with all research regulations including HIPAA ICH and GCP guidelines
- Maintains strictest confidentiality with regards to patient information
- Participates in staff meetings as directed by the Primary Investigator or Research Manager
- Cross trains and performs other functions as directed by the Primary Investigator and Research Manager
- Any other duties and / or special projects as assigned
Qualifications
REQUIRED EDUCATION SKILLS AND EXPERIENCE
Bachelors degree required. Minimum of one year of clinical research experience required. Research Coordinator must be computer literate and able to operate healthcare system multiple Microsoft Office applications and study-specific protocol software. Must be experienced in phlebotomy specimen collection processing and shipping.
ADDITIONAL SKILLS AND EXPERIENCE
Research Coordinator must be able to :
Provide a high level of quality patient care and customer service at all timesPlan prioritize and complete multiple tasks as delegated by the Primary Investigator or Research ManagerWork under pressure; assess respond to and communicate issues in a timely mannerMaintain composure and set a professional example to patients and coworkersCommunicate clearly with patients and coworkers through the telephone email and in-personInterpret and apply clinical and non-clinical policies and proceduresBe reliable punctual and able to work independently and with flexibility to accommodate protocol requirementsRequired Experience :
IC
Key Skills
CSS,Cloud Computing,Health Education,Actuary,Building Electrician
Employment Type : Full-Time
Experience : years
Vacancy : 1