Current jobs related to Clinical Trials Nursing Coordinator - New Brunswick, New Jersey - Actalent
-
Clinical Trials Coordinator
2 weeks ago
New Brunswick, New Jersey, United States Actalent Full timeJob Title:Clinical Trials SpecialistJob Summary:Actalent is seeking a highly skilled Clinical Trials Specialist to join our team. As a Clinical Trials Specialist, you will play a critical role in the initiation, activation, and ongoing management of clinical trials.Key Responsibilities:Collaborate with various departments to prepare and review study tools,...
-
Clinical Research Coordinator
5 days ago
New Brunswick, New Jersey, United States Vitalief Full timeWhy Choose Vitalief?Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Our mission is to provide cutting-edge solutions to clients in the research and clinical trial industry.We prioritize personal and professional growth for all Vitalief employees, fostering a culture that encourages innovation and collaboration.Our...
-
Clinical Research Coordinator
1 week ago
New Brunswick, New Jersey, United States Vitalief Full timeJob OverviewVitalief is a pioneering consultancy addressing the healthcare human capital epidemic. We are seeking a highly skilled Clinical Research Coordinator to join our team and contribute to the success of our clients in the research and clinical trial industry.Key Responsibilities:Manage eligibility check lists, perform patient screening/consenting,...
-
Clinical Research Coordinator
5 days ago
New Brunswick, New Jersey, United States Vitalief Full timeJob Summary:Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Our team is dedicated to helping clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions.Key Responsibilities:Assist with monitoring patient visits and tracking deviations and documenting SAEs (serious...
-
Senior Financial Analyst, Clinical Trials
5 days ago
New Brunswick, New Jersey, United States Vitalief Full timeJob OverviewVitalief is seeking a highly skilled Senior Financial Analyst to join our team. As a key member of our Clinical Trials department, you will be responsible for preparing, maintaining, and negotiating budgets related to clinical trial activities.Key ResponsibilitiesPrepare and maintain clinical trial budgets, ensuring compliance with CMS National...
-
Clinical Trials Director
1 week ago
New Brunswick, New Jersey, United States Vitalief Full timeJob DescriptionVitalief is a pioneering research and clinical trial solutions consulting company seeking a strategic solutions professional to join our client services delivery team. As a Director, Clinical Trials, you will work closely with senior management and business development to identify innovative ways to deliver services to clients. Your...
-
Clinical Trials Director
1 month ago
New Brunswick, New Jersey, United States Vitalief Full timeJob OpportunityVitalief is a pioneering research and clinical trial solutions consulting company seeking a strategic solutions professional to join our exceptional client services delivery team. As a Director of Clinical Trials, you will work closely with senior management and our business development team to identify and recommend innovative ways of...
-
Senior Clinical Research Coordinator
5 days ago
New Brunswick, New Jersey, United States Vitalief Full timeSenior Clinical Research CoordinatorVitalief is seeking a highly skilled Senior Clinical Research Coordinator to join our team. As a key member of our research team, you will be responsible for coordinating clinical trials, ensuring compliance with regulatory requirements, and providing exceptional patient care.Key Responsibilities:Coordinate clinical...
-
Clinical Trial Associate II
2 weeks ago
New Brunswick, New Jersey, United States Allen Spolden Full timeJob Title: Clinical Trial Associate IIAllen Spolden is seeking a highly skilled Clinical Trial Associate II to support the operational strategy and execution of clinical studies. The successful candidate will work closely with the Clinical Operations Manager, study teams, and Clinical Research Organizations (CROs) to ensure the successful delivery of...
-
Senior Clinical Research Associate
2 weeks ago
New York, New York, United States Worldwide Clinical Trials Full timeJoin Our Team at Worldwide Clinical TrialsWe are a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications.Our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases enables us to...
-
Clinical Trial Associate
2 weeks ago
New Brunswick, New Jersey, United States Allen Spolden Full timeJob DescriptionThe Clinical Trial Associate will play a crucial role in supporting the operational strategy and execution of clinical studies at Allen Spolden. This position will work closely with the Clinical Development Plan to ensure seamless study execution.Key Responsibilities:Provide support for daily clinical study activities, including regulatory...
-
Clinical Trial Associate
1 week ago
New Brunswick, New Jersey, United States Allen Spolden Full timeJob SummaryThe Clinical Trial Associate - Study Support will play a key role in supporting the operational strategy and execution of clinical studies at Allen Spolden. This position will work closely with the Clinical Operations Manager, study teams, and Clinical Research Organizations (CROs) to ensure the successful execution of clinical trials.Key...
-
Clinical Research Coordinator
3 weeks ago
New Brunswick, New Jersey, United States Vitalief Full timeJob Title: Clinical Research CoordinatorAbout the Role:Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. We are seeking a highly skilled Clinical Research Coordinator to join our team and contribute to our mission of adapting to evolving requirements in the research and clinical trial industry with cutting-edge...
-
Clinical Trials Payment Coordinator
3 weeks ago
New York, New York, United States Collabera Full timeAbout the Role:We are seeking a highly skilled Clinical Trials Payment Coordinator/Site Payment Coordinator to support our team in a 100% remote role. The ideal candidate will be located on the East coast and have a strong understanding of clinical site payments.Responsibilities:Support site payment-related activities for clinical trials, ensuring accurate...
-
Senior Clinical Research Coordinator
2 weeks ago
New Brunswick, New Jersey, United States Vitalief Full timeJob OverviewVitalief is seeking a highly skilled Senior Clinical Research Coordinator to join our team. As a key member of our research team, you will be responsible for coordinating and managing clinical trials, ensuring compliance with regulatory requirements, and providing exceptional patient care.Key ResponsibilitiesCoordinate and manage clinical trials,...
-
Clinical Research Nurse Coordinator
6 days ago
New Brunswick, New Jersey, United States MaineHealth Full timeJob SummaryThis position is for a skilled Registered Nurse to join our team at the MaineHealth Institute for Research, contributing to biomedical research in the area of Oncology. Our team is specifically interested in therapeutic trials testing various combinations of chemotherapy, immunotherapy, targeted therapy, and radiation therapy.Key...
-
Clinical Research Nurse Coordinator
1 month ago
New Brunswick, New Jersey, United States MaineHealth Full timeJob SummaryThis position is part of a dynamic team at the MaineHealth Institute for Research, contributing to biomedical research in the area of Oncology. We are seeking a highly organized and detail-oriented Clinical Research Nurse Coordinator to join our team.Key ResponsibilitiesPre-screen and enroll patients for research studiesSchedule study assessments...
-
Clinical Trials Manager
5 days ago
New York, New York, United States Mount Sinai Health System Full timeClinical Trials Manager Job SummaryThe Mount Sinai Health System is seeking a highly skilled Clinical Trials Manager to coordinate and manage multiple clinical trial projects and protocols. This role will oversee the coordination of clinical trials, including federally funded studies, investigator-initiated studies, and those from pharmaceutical...
-
Clinical Research Nurse Coordinator
1 month ago
New Brunswick, New Jersey, United States MaineHealth Full timeJob SummaryThis position is an exciting opportunity to join a dynamic team at the MaineHealth Institute for Research, contributing to biomedical research in the area of Oncology. Our team is focused on therapeutic trials testing various combinations of chemotherapy, immunotherapy, targeted therapy, and radiation therapy.Key ResponsibilitiesPre-screen and...
-
Clinical Trials Manager
2 weeks ago
New York, New York, United States Mount Sinai Health System Full timeAbout the RoleWe are seeking a highly skilled Clinical Trials Manager to join our team at Mount Sinai Health System. As a Clinical Trials Manager, you will be responsible for coordinating and managing multiple clinical trials projects and protocols, including those from pharmaceutical companies.Key ResponsibilitiesManage and coordinate assigned clinical...
Clinical Trials Nursing Coordinator
2 months ago
Position Title:
Clinical Research Nurse Coordinator
Role Overview:
As a Clinical Research Nurse Coordinator, you will work closely with the Protocol Activation office to facilitate the initiation and activation of new clinical trial protocols. Your role encompasses the preparation and assessment of study tools, confirmation of necessary approvals, and the delivery of nursing education. You will also be responsible for coordinating study enrollment by pre-screening potential participants, securing informed consent, and ensuring meticulous documentation.
Key Responsibilities:
- Oversee the preparation and evaluation of study instruments.
- Confirm all necessary approvals are in place.
- Manage the informed consent process.
- Execute protocol-specific nursing orders and coordinate patient care.
- Document adverse events and maintain research records.
- Collaborate effectively with medical system personnel.
- Ensure compliance with regulatory standards and promote professional development.
Essential Skills:
Hard Skills:
- Proficient in study tool preparation and review.
- Skilled in verification of approvals.
- Knowledgeable in the informed consent process.
- Experienced in executing protocol-specific orders.
- Competent in adverse event documentation and database management.
Soft Skills:
- Strong collaboration abilities.
- Excellent communication skills with patients.
- Effective problem-solving capabilities.
- Team-oriented mindset.
- Commitment to professional responsibility and ongoing education.
Employment Type:
This position is classified as Contract-to-Hire.
Work Environment:
Actalent is dedicated to leading advancements in scientific discovery, patient care, and education aimed at improving cancer outcomes. Our approach is rooted in innovative research and patient-centered care, supported by disease-specific groups, quality assurance, informatics, education, and finance. With a robust team and extensive enrollment needs, we manage numerous active trials focused on enhancing cancer prevention and developing improved therapies.
About Actalent:
Actalent stands as a global leader in engineering and scientific services, providing talent solutions that empower visionary companies to advance their initiatives through specialized expertise. With a vast network of consultants and clients across multiple regions, Actalent is committed to fostering diversity, equity, and inclusion within its workforce, ensuring a culture that promotes growth and recognition for all individuals.
