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Senior Clinical Research Coordinator
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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...
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Clinical Research Coordinator
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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...
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Clinical Research Coordinator
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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’...
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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’...
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Clinical Research Coordinator
1 month 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 Coordinator to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our...
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Experienced Clinical Research Manager
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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...
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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...
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Clinical Research Associate
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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...
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Healthcare Research Coordinator
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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...
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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...
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Clinical Research Study Manager
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Clinical Research Study Manager
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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’...
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Clinical Research Study Supervisor
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Clinical Research Study Manager
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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...
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Oncology Clinical Research Supervisor
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Research Manager
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Research Nurse
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Newark, United States University of Delaware Full timeGrade: 30E CONTEXT OF THE JOB The COBRE in Cardiovascular Health is seeking a Research Nurse to support several investigations related to cardiovascular health in children through seniors. The Research Nurse will provide nursing support and assist in the coordination of COBRE related clinical research projects by performing/assisting with medical...
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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...
Senior Clinical Research Coordinator
2 months ago
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.
Work Location: Work is 5 days per week on-site in Newark, NJ. Possibility of working one day remote per week after acclimated.
Responsibilities:
- Under supervision of clinical research leadership staff, the medical staff, and in collaboration with research nurse staff, performs protocol-specific tasks including patient screening, ordering tests, collecting specimens and study documentation of patient reported responses, relative to various Oncology trials.
- Serves as a liaison (Communicating effectively) between the organization, investigators, members of the research team (i.e., physicians, nurses, hospital, and laboratory staff), and the research sponsors - to ensure that services are coordinated and delivered to patients in a timely manner.
- Maintains research record (e.g., patient consent, eligibility, Case Report Forms (CRF), registration confirmation, corresponding source documents, etc.) for all patients enrolled in Oncology trials.
- Participates in site preparation for trials including protocol feasibility, preliminary study budget, startup meeting preparation, training staff, and preparation of IRB applications and preparation of regulatory documents, study documents and forms.
- Schedules and conducts trial visits by informing patients and coordinating procedures per protocol.
- Assesses and triages study patients appropriately for serious/unexpected adverse events (SAE), reports and records adverse events according to all applicable regulation and study protocol.
- Assists patients in understanding their diagnosis, treatment options, and the resources available including educating eligible patients about appropriate clinical research studies and technologies.
- Bachelor's Degree required.
- Minimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within reporting deadlines outlined in the protocol.
- Oncology clinical research experience is a huge plus.
- Strong working knowledge of current Code of Federal Regulation and Good Clinical Practice guidelines.
- Compassionate personality and ability to interact with patients in a clear and confident manner.
- Ability to work on several trials concurrently - can demonstrate versatility, "can do" attitude, and possess strong organizational, time management and prioritization skills.
- Ability to work collaboratively with all team members (i.e., physicians, nurses, hospital, and laboratory staff) to ensure that services are coordinated and delivered to patients in a timely manner.
- Needs to be communicative and responsive and know when to escalate and communicate issues to management.
- Capable of independent decision-making, and able to thrive in a fast-paced environment working on multiple clinical trials concurrently.
- Must have strong Microsoft Office skills.
- Any exposure to EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus.
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.
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