Current jobs related to Senior Clinical Research Coordinator - New Brunswick - Vitalief


  • New York, New York, United States Tandem Clinical Research Full time

    Job Title: Clinical Research CoordinatorTandem Clinical Research is a leading clinical research company dedicated to advancing medical knowledge and improving patient outcomes. We are seeking a highly skilled Clinical Research Coordinator to join our New York team.Job SummaryThe Clinical Research Coordinator will play a critical role in the success of our...


  • New York, New York, United States Tandem Clinical Research Full time

    Job SummaryTandem Clinical Research is a leading clinical research organization dedicated to advancing medical knowledge through the conduct of clinical trials. We are seeking a highly skilled Clinical Research Coordinator to join our team in New York.Key ResponsibilitiesOversee and coordinate the daily activities of clinical research studies, ensuring...


  • New York, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionClinic Research Coordinator II The Clinical Research Coordinator II, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study...


  • New Brunswick, United States Vitalief Full time

    Job 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...


  • New Brunswick, United States Vitalief Full time

    Job 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...


  • New Brunswick, United States Vitalief Full time

    Job 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...


  • New York, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionUnblinded Clinical Research Coordinator IDM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.Duties & Responsibilities:Compound and dispense prescribed IP.    ...


  • New York, United States Tandem Clinical Research Full time

    Tandem Clinical Research is a clinical research company dedicated to testing investigational medications and devices that cover a broad range of diseases and disorders. We are actively seeking a Bilingual Clinical Research Coordinator to join our New York Team.JOB DESCRIPTIONThe Clinical Research Coordinator oversees and coordinates the daily activities of...


  • New York, United States Tandem Clinical Research Full time

    Tandem Clinical Research is a clinical research company dedicated to testing investigational medications and devices that cover a broad range of diseases and disorders. We are actively seeking a Bilingual Clinical Research Coordinator to join our New York Team.JOB DESCRIPTIONThe Clinical Research Coordinator oversees and coordinates the daily activities of...


  • new york city, United States Tandem Clinical Research Full time

    Tandem Clinical Research is a clinical research company dedicated to testing investigational medications and devices that cover a broad range of diseases and disorders. We are actively seeking a Bilingual Clinical Research Coordinator to join our New York Team.JOB DESCRIPTIONThe Clinical Research Coordinator oversees and coordinates the daily activities of...


  • new york city, United States Tandem Clinical Research Full time

    Tandem Clinical Research is a clinical research company dedicated to testing investigational medications and devices that cover a broad range of diseases and disorders. We are actively seeking a Bilingual Clinical Research Coordinator to join our New York Team.JOB DESCRIPTIONThe Clinical Research Coordinator oversees and coordinates the daily activities of...


  • New York, United States Evolution Research Group Full time

    ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400+...


  • New York, United States Evolution Research Group Full time

    ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400+...


  • New Brunswick, New Jersey, United States Vitalief Full time

    Job OverviewAbout 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 Senior Clinical Research Coordinator to contribute to our mission of making a significant impact on patient lives.Why Choose Vitalief?Play a vital role in...


  • New York, New York, United States US Tech Solutions Full time

    Job Title: Senior Clinical Research CoordinatorDuration: 12 Months (Possibility of Extension)Job Summary:The Senior Clinical Research Coordinator will be responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, and documenting and reporting on the daily operations of assigned trials....


  • New Brunswick, New Jersey, United States Vitalief Full time

    Job 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 Senior Clinical Research Coordinator to become a vital part of our dynamic team, fully committed to our mission of making a significant impact on lives through our...


  • new york city, United States Evolution Research Group Full time

    ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400+...


  • New York, New York, United States Tandem Clinical Research Full time

    Tandem Clinical Research is a clinical research organization dedicated to conducting clinical trials for investigational medications and devices that cover a broad range of diseases and disorders.**Job Summary**The **Sub-Investigator** will act as a clinical investigator in a clinical trial setting. As an advanced practice medical professional, you will be...


  • New York, New York, United States Tandem Clinical Research Full time

    Clinical Research Opportunities at Tandem Clinical ResearchJob Title: Sub-InvestigatorJob Summary: Tandem Clinical Research is seeking a skilled Sub-Investigator to join our New York team. As a Sub-Investigator, you will play a critical role in conducting clinical trials and ensuring the highest level of patient care.Key Responsibilities:* Conduct physical...


  • New Brunswick, New Jersey, United States Allen Spolden Full time

    Position Overview As a Senior Clinical Research Specialist at Allen Spolden, you will play a pivotal role in supporting clinical trials by providing comprehensive research assistance. This position involves collaboration with the clinical study team under the guidance of a supervisor or designated leader. Key Responsibilities Contribute to the design and...

Senior Clinical Research Coordinator

3 months ago


New Brunswick, United States Vitalief Full time
Job DescriptionJob Description

WHY 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 growth for all Vitalief employees.
  • We give everyone a seat at the table – we encourage innovation.
  • We’re committed to our employees – you are encouraged and mentored by the talented Vitalief team to achieve full potential.
  • “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:  $75,000 to $90,000 annually

Work Location:  Work is 5 days per week on-site in New Brunswick, NJ.  Ability to work one day remote per week after acclimated.

Responsibilities:

  • Under the direct supervision of the Nurse Manager of Clinical Research Center, performs patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, data management. and other clinical trial activities for solid tumor, high enrollment, adult population Oncology related trials.
  • Serves as a liaison 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.
  • 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.

Required Skills:

  • 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/pre-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.
  • Bachelor’s Degree required.
  • Oncology clinical research experience is required.
  • Any experience working with solid tumors is a big plus.
  • 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.

PHYSICAL DEMANDS: Standing, sitting for long periods of time working on a computer, visual perception, walking, talking and hearing. Lifting up to 25lbs.

IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

#LI-DNI

 

Powered by JazzHR

ni3tHmnivb