What are the responsibilities and job description for the Junior Clinical Research Coordinator position at Vitalief Inc.?
Overview
Vitalief is a leading site solutions partner focused on improving the value and contribution of clinical trial sites across the drug development lifecycle. We offer integrated Consulting (strategic and operational), Functional Service Provider (FSP) services, Workforce Solutions (training and career pathing), and Site Networks that enhance clinical trials and improve patient outcomes. We are seeking a Junior Clinical Research Coordinator (CRC) that is interested in spearheading the research of a variety of Tuberculosis trials with one of our exceptional client teams and gaining lifetime hands on experience.
WHY VITALIEF?
Work Location: Hybrid; Occasional travel to Newark, NJ.
Responsibilities
IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
Vitalief is a leading site solutions partner focused on improving the value and contribution of clinical trial sites across the drug development lifecycle. We offer integrated Consulting (strategic and operational), Functional Service Provider (FSP) services, Workforce Solutions (training and career pathing), and Site Networks that enhance clinical trials and improve patient outcomes. We are seeking a Junior Clinical Research Coordinator (CRC) that is interested in spearheading the research of a variety of Tuberculosis trials with one of our exceptional client teams and gaining lifetime hands on experience.
WHY VITALIEF?
- You can actively contribute to our clients’ mission of advancing scientific discoveries that have the potential to change patients' lives for the better.
- Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees.
- We give everyone a seat at the table – we encourage innovation.
- Life/work balance that includes 20 PTO (Paid Time Off) days plus 9 paid Holidays annually.
- Other benefits include Company paid life insurance and short / long term disability coverage; 401K retirement program; Robust healthcare plans to choose from.
Work Location: Hybrid; Occasional travel to Newark, NJ.
Responsibilities
- Provide oversight and management of potential study participants
- Coordinate the flow of patients and patient retention throughout the life of the study
- Oversee study data collection and management
- Manage the enrolling and consenting of participants
- Maintain up to date knowledge of IRB protocol and report to IRB offices
- Attend monthly study meetings
- Minimum of 1 years working in research
- Bachelors degree in a related field (e.g., life sciences, public health, healthcare administration).
- Experience working with phlebotomy blood draws a plus
- Bilingual in Spanish preferred
- Critical thinking and decision-making skills – ability to evaluate all aspects of a situation and to independently make appropriate and timely decisions.
- Excellent oral and written communication, presentation and interpersonal skills.
- Strong proficiency in Microsoft Office Suite and computer-based information systems.
IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
Salary : $45,000 - $50,000