Current jobs related to Clinical Research Operations Manager - Newark - Vitalief
-
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...
-
Oncology Clinical Research Manager
4 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...
-
Oncology Clinical Research Manager
7 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...
-
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 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 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...
-
Experienced Clinical Research Manager
7 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...
-
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...
-
Clinical Research Project Manager
1 week 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
7 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 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’...
-
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...
-
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 Supervisor
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 Supervisor to join our exceptional team (as full-time, fully benefited Vitalief employee) to support...
-
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
2 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. This role is designed for a full-time, fully benefited employee who...
-
Clinical Trials Operations Supervisor
1 week ago
Newark, New Jersey, United States Vitalief Inc. Full timeJOIN 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 a vital part of our outstanding team. This full-time position comes with comprehensive benefits, aligning with our...
-
Research Manager
4 weeks ago
Newark, United States ChristianaCare Full timeDo you want to work at one of the Top 100 Hospitals in the nation? We are guided by our values of Love and Excellence and are passionate about delivering health, not just health care. Come join us at ChristianaCare!ChristianaCare is searching for a Research Manager to provide supervision and leadership to the ChristianaCare (CC) Oncology Pharmaceutical...
Clinical Research Operations Manager
2 months 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 Operations Manager 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:
Work is four (4) days per week on-site in
Newark, NJ
and one (1) day remote.
Responsibilities:
Establish workflows and processes to support high-quality clinical research activities, serving as the primary liaison between Vitalief’s client (an Oncology research institution) local sites and their Office of Human Research Services.
Assures that all clinical research conducted is according to Good Clinical Practice (GCP) guidelines as well as applicable Institutional, State and Federal regulations and guidelines. In addition, this position is responsible for meeting the goals and objectives established by the management team.
Interacts and establishes appropriate with affiliate medical staff, executive staff, department heads and others to coordinate activities, expand services, establish efficiencies, resolve conflicts and foster an atmosphere of teamwork and cooperation.
Provides day-to-day supervision of clinical research staff including support, guidance and training consistent with staff needs, relative to clinical trial activities.
Demonstrates leadership in examining staffing patterns, schedules, and making recommendations to ensure appropriate staff coverage and utilization of staff.
Works closely with the Management team in developing, implementing and evaluating standard operating procedures to support the clinical research program.
Ensures clinical research processes are patient centered.
Performs Quality Assurance audits regularly with the assigned team to ensure that the data collected is completed and accurate and to ensure that the research project, database or protocol is carried out as outlined.
Ensures that research protocols are approved by the Institutional Review Board and all regulatory documentation is completed prior to the initiation of the protocol.
Works collaboratively with physician colleagues, nurses, pharmacy, reception staff, partnering staff and all members of the Office of Human Research Services, appropriate hospital and laboratory staff to ensure that services are coordinated and delivered to patients in a timely manner.
Maintains working knowledge of DHHS, FDA, OHRP, NIH, GCP, HIPAA, IRB and other applicable guidelines.
Required Skills:
Bachelor’s Degree in a social science or related field.
5 years of experience working in a clinical research institution (as opposed to working for a Sponsor and/or CRO).
3 years of Oncology research experience.
One to two years of supervisory experience in a clinical research environment. Supervision in a unionized environment is a plus.
Solid leadership and people management skills; ability to foster a positive work environment.
Strong verbal and written communication skills and ability to form cross functional leadership partnerships to accomplish goals.
Organizational and time management skills. Collaborative, energetic, team-oriented professional who is comfortable with change.
Capable of independent decision-making, and able to thrive in a fast-paced environment working on multiple clinical trials concurrently.
Association of Clinical Research Professional (ACRP) certification or Society of Clinical Research Associates (CCRP) certification required.
Advanced Microsoft office skills (Word, PowerPoint, and Excel); electronic medical record/EPIC and Clinical Trials Management System (e.g., Velos, OnCore) experience.
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.
#J-18808-Ljbffr
