Vitalief
Senior Clinical Research Coordinator
Vitalief, Livingston, New Jersey, us, 07039
WHY VITALIEF?
Vitalief is emerging as an innovative Healthcare consulting company, focused on empowering Research and transforming Clinical Trials. As a result, we are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’ mission to impact and save lives.
Reasons to work for 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.
Salary Range: Market competitive - based on experience level.
Work Location: On-site in Livingston, NJ
Responsibilities:
Strong understanding and knowledge base of coordination requirements associated with clinical research trials.
Ability to interface effectively with all levels of management and work and communicate with both internal and external customers.
Ability to work and make decisions independently.
Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint, and Outlook.
Familiar with internet applications.
Effective oral, written communication and interpersonal skills.
Excellent time management skills with the ability to multi-task.
Required Skills:
A Bachelor’s Degree or equivalent in Business Administration, Health Care Administration or related discipline.
A minimum of three-four years of progressively responsible related experience coordinating clinical research trials studies.
Responsible for initiating, coordinating and managing research studies including but not limited to research responsibilities with the client’s Health Assessment Center for Athletes.
Oversees the financial and protocol development for assigned studies.
Assists with managing the recruitment process (develops advertising strategy, contacts media outlets and negotiates rates and monitors deadlines for submission of materials), enrollment, grant submissions, and study coordination.
Performs intra-operative monitoring and serves as liaison with internal and external funding agencies.
Oversees and executes all research IRB projects associated with identified focus areas collaboratively with hospital division and versed in following hospital IRB protocol, policies, and procedures.
Ensures the accurate execution of research protocols in accordance with Good Clinical Practices, HIPAA and required obligations to patient/subject, Principal Investigator, research team and the Sponsor.
Interfaces directly with patients/subjects and the Principal Investigator in support of the clinical trials if applicable.
Provides guidance to Research support staff.
Works autonomously and with limited oversight on projects in coordination with the Chief Medical Officer, the Health Assessment Center for Athletes and Associated Hospital Clinical Leadership.
PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs.
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.
#LI-DNI
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Vitalief is emerging as an innovative Healthcare consulting company, focused on empowering Research and transforming Clinical Trials. As a result, we are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’ mission to impact and save lives.
Reasons to work for 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.
Salary Range: Market competitive - based on experience level.
Work Location: On-site in Livingston, NJ
Responsibilities:
Strong understanding and knowledge base of coordination requirements associated with clinical research trials.
Ability to interface effectively with all levels of management and work and communicate with both internal and external customers.
Ability to work and make decisions independently.
Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint, and Outlook.
Familiar with internet applications.
Effective oral, written communication and interpersonal skills.
Excellent time management skills with the ability to multi-task.
Required Skills:
A Bachelor’s Degree or equivalent in Business Administration, Health Care Administration or related discipline.
A minimum of three-four years of progressively responsible related experience coordinating clinical research trials studies.
Responsible for initiating, coordinating and managing research studies including but not limited to research responsibilities with the client’s Health Assessment Center for Athletes.
Oversees the financial and protocol development for assigned studies.
Assists with managing the recruitment process (develops advertising strategy, contacts media outlets and negotiates rates and monitors deadlines for submission of materials), enrollment, grant submissions, and study coordination.
Performs intra-operative monitoring and serves as liaison with internal and external funding agencies.
Oversees and executes all research IRB projects associated with identified focus areas collaboratively with hospital division and versed in following hospital IRB protocol, policies, and procedures.
Ensures the accurate execution of research protocols in accordance with Good Clinical Practices, HIPAA and required obligations to patient/subject, Principal Investigator, research team and the Sponsor.
Interfaces directly with patients/subjects and the Principal Investigator in support of the clinical trials if applicable.
Provides guidance to Research support staff.
Works autonomously and with limited oversight on projects in coordination with the Chief Medical Officer, the Health Assessment Center for Athletes and Associated Hospital Clinical Leadership.
PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs.
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.
#LI-DNI
Powered by JazzHR