Clinical Research Coordinator
1 month ago
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 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.
Work Location: Newark, NJ. This job is 100% remote – however candidates MUST reside either in NY, NJ, CT or PA to be considered for this position Ability to travel internationally up to 30% - to South America, Africa or Europe, two to three times per year.
Responsibilities:
- Under the direction of the Principal Investigator(s), Data and Operations Management Director and Associate Director, and other leadership within the Infectious Diseases department, this resource will perform various research operations for specific assigned observational clinical studies (meaning patients are NOT being treated in a clinical trial).
- Implement and monitor quality control SOPs and conduct periodic monitoring visits working with investigators at the sites to develop and implement protocols.
- Assist in the establishment of standard operating procedures and manuals of operations for clinical studies.
- Assist with the instructing and training of student research assistants and temporary research assistants in study document preparation and study-start-up procedures to develop the skills necessary to perform the required functions. Assist in training local site clinicians on study protocols.
- Oversee and administer protocols and translate protocols into operational implementation and conduct at the foreign and domestic sites. Site locations include, but are not limited to: North America, Peru, Brazil, Moldova, Uganda, Kenya, South Africa, India, Vietnam, Indonesia, China, and the Philippines.
- Assure timely responses to study inquiries and schedule regular “monitoring” visits.
- Oversee quality assurance/quality control activities with on-site staff and investigators.
- Assists faculty in developing study patient consent forms & applications to the IRB. Responsible for reporting protocol changes to the IRB.
- Provide specialized protocol, procedure and application (REDCap, FreezerPro specimen tracking) training to international site study team (investigators and staff).
- Bachelor’s Degree plus three (3) years of scientific/clinical research experience OR Master’s Degree plus two (2) years of scientific/clinical research experience.
- Experience overseeing administering protocols and translating protocols into operational implementation and conduct at the foreign and domestic sites.
- Experience Implementing and monitoring quality control SOPs and conducting periodic monitoring visits working with investigators at the sites to develop and implement protocols.
- Confident in ability to train junior research assistants in study document preparation and study-start-up procedures to develop the skills necessary to perform the required functions.
- Infectious disease experience is a plus (not a requirement).
- Ability to travel 6 weeks yearly – consisting of two to three 2-week trips to either South America, Africa, Europe, and/or Asia.
- Strong relationship building and interpersonal skills.
- Effective oral and written communication skills.
- Excellent organizational skills and attention to detail.
- Computer literacy with proficiency and working knowledge of database and reporting tools such as Microsoft Word, Excel, Access and PowerPoint.
PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs. Ability to travel internationally up to 30% - to South America, Africa or Europe, two to three times per year.
#LI-DNI
Powered by JazzHR
xR0qsuZDuE
-
Clinical Research Coordinator
3 months ago
Newark, United States Vitalief Full timeJob DescriptionJob DescriptionWHY VITALIEF?Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief:Our PEOPLE FIRST culture prioritizes personal and professional...
-
Senior Clinical Research Coordinator
2 months ago
Newark, United States Vitalief Full timeJob DescriptionJob DescriptionWHY 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...
-
Lead Clinical Research Coordinator
12 hours ago
Newark, New Jersey, United States Vitalief Full timePosition OverviewWhy Choose Vitalief?Vitalief is at the forefront of Healthcare consulting, dedicated to enhancing Research and revolutionizing Clinical Trials. We are in search of a skilled and passionate Senior Clinical Research Coordinator to become a vital part of our outstanding team. This role is designed for a full-time, fully benefited employee who...
-
Clinical Research Coordinator
1 month ago
Newark, United States Vitalief Inc. Full timeWHY 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 Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’...
-
Clinical Research Coordinator
1 month ago
Newark, United States Vitalief Inc. Full timeWHY 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 Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’...
-
Experienced Clinical Research Manager
6 days ago
Newark, New Jersey, United States Vitalief Full timePosition OverviewWhy Choose Vitalief?Vitalief is at the forefront of Healthcare consulting, dedicated to enhancing Research and revolutionizing Clinical Trials. We are in search of a skilled and passionate Senior Clinical Research Coordinator to become a vital part of our outstanding team, committed to our mission of making a significant impact on lives...
-
Healthcare Research Coordinator
16 hours ago
Newark, New Jersey, United States Vitalief Full timeJoin Our Team at Vitalief ConsultingCompany Overview:Vitalief Consulting stands at the forefront of healthcare human capital solutions, dedicated to enhancing the research and clinical trial landscape. We invite you to be part of our innovative team and make a significant impact in the industry.Why Work with Us?We foster a culture that emphasizes both...
-
Oncology Clinical Research Manager
2 days ago
Newark, New Jersey, United States Vitalief Full timeJob OverviewWHY VITALIEF?Vitalief is a forward-thinking Healthcare consulting firm dedicated to enhancing Research and revolutionizing Clinical Trials. We are in search of a skilled and passionate Clinical Research Study Manager to become a vital part of our dedicated team, contributing to our mission and that of our clients to make a meaningful impact on...
-
Clinical Research Study Manager
4 weeks ago
Newark, United States Vitalief Full timeJob DescriptionJob DescriptionWHY 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 Clinical Research Study Manager to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our...
-
Clinical Research Study Manager
2 months ago
Newark, United States Vitalief Inc. Full timeWHY 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 Clinical Research Study Manager to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’...
-
Clinical Research Study Supervisor
3 weeks ago
Newark, United States Vitalief Full timeJob DescriptionJob DescriptionWHY 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 Clinical Research Study Supervisor to join our exceptional team (as full-time, fully benefited Vitalief employee) to support...
-
Clinical Research Study Supervisor
4 weeks ago
Newark, United States Vitalief Inc. Full timeWHY 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 Clinical Research Study Supervisor to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’...
-
Clinical Research Study Manager
2 months ago
Newark, United States Vitalief Inc. Full timeWHY 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 Clinical Research Study Manager to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’...
-
Clinical Research Project Manager
6 days ago
Newark, New Jersey, United States Vitalief Full timeJoin Our Team at Vitalief ConsultingCompany Overview:Vitalief Consulting is a premier consultancy dedicated to providing healthcare human capital solutions. Become a part of our innovative team and play a key role in advancing the research and clinical trial landscape.Why Work with Us?We foster a culture that emphasizes both personal and professional...
-
Oncology Clinical Research Supervisor
6 days ago
Newark, New Jersey, United States Vitalief Inc. Full timeWHY CHOOSE VITALIEF INC.?Vitalief Inc. is at the forefront of Healthcare consulting, dedicated to enhancing Research and revolutionizing Clinical Trials. We are on the lookout for a skilled and passionate Clinical Research Study Supervisor to become an integral part of our dynamic team. As a full-time employee, you will play a crucial role in our mission to...
-
Clinical Trials Senior Coordinator
12 hours ago
Newark, New Jersey, United States Vitalief Full timePosition OverviewWhy Choose Vitalief?Vitalief is at the forefront of Healthcare consulting, dedicated to enhancing Research and revolutionizing Clinical Trials. We are on the lookout for a skilled and passionate Senior Clinical Research Coordinator to become a vital part of our remarkable team (as a full-time, fully benefited employee) to further our mission...
-
Newark, New Jersey, United States Vitalief Full timeJob OverviewWHY VITALIEF?Vitalief is at the forefront of Healthcare consulting, dedicated to enhancing Research and revolutionizing Clinical Trials. We are in search of a skilled and passionate Clinical Research Study Manager to contribute to our mission and assist our clients in making a significant impact on patient lives.Benefits of Working at...
-
Clinical Research Associate
1 month ago
Newark, United States QPS, LLC Full timeJob DescriptionJob DescriptionDo you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As a Clinical Research Associate (CRA) or Senior CRA with QPS’ Global Project Management Office (cPMO), you’ll be at the heart of our mission to enhance patient health by...
-
Clinical Research Associate
4 weeks ago
Newark, United States QPS, LLC Full timeJob DescriptionJob DescriptionDo you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As a Clinical Research Associate (CRA) or Senior CRA with QPS’ Global Project Management Office (cPMO), you’ll be at the heart of our mission to enhance patient health by...
-
Oncology Clinical Research Manager
6 days ago
Newark, New Jersey, United States Vitalief Full timeJob OverviewWHY VITALIEF?Vitalief is a pioneering Healthcare consulting firm dedicated to enhancing Research and revolutionizing Clinical Trials. We are in search of a skilled and passionate Clinical Research Study Manager to become a vital part of our dynamic team, committed to our mission of making a significant impact on patient lives.Benefits of Working...
