Travel Clinical Research Coordinator - $1,020 per week
Company: TalentBurst, Inc
Location: New York
Posted on: April 28, 2024
Job Description:
TalentBurst, Inc is seeking a travel Clinical Research
Coordinator for a travel job in New York, New York.Job Description
& Requirements
- Specialty: Clinical Research Coordinator
- Discipline: Allied Health Professional
- Start Date: 07/01/2024
- Duration: 26 weeks
- 40 hours per week
- Shift: 8 hours
- Employment Type: TravelPURPOSE AND SCOPE: Works under the
supervision of the Principal Investigator (PI), Director and other
site personnel as applicable. Conceptually applies the research
protocol to the clinical setting to allow accurate and timely
completion of all duties. Maintains appropriate documentation
associated with the assigned clinical study. Ensures studies are
conducted according to established company policies and procedures
as well as all applicable State and Federal regulations,
specifically Good Clinical Practice (GCP), ICH, and FDA guidelines.
PRINCIPAL DUTIES AND RESPONSIBILITIES: --- Develops in-depth
understanding of each study protocol to ensure all aspects of the
protocol are adhered to in accordance with FDA, GCP, and ICH
Guidelines. --- Under the supervision of the Principal Investigator
(PI) and appropriate management prepares and submits regulatory
documents in an accurate and timely manner. --- In collaboration
with the PI, incorporates clinical judgment and knowledge of
protocol to identify potential study participants according to
inclusion and exclusion criteria. --- Obtains informed consent
according to GCP. --- Schedules subject visits. --- Prepares
labs/tests per protocol. --- Responsible for study drug storage and
drug accountability according to the parameters of the study
protocol and sponsor requirements. --- Administers the
investigational product according to the parameters of the study
protocol and under the direction of the physician. LVNs/LPNs may
administer medications under their state licensure and under the
order of the PI. Non-LVNs may administer oral and subcutaneous
drugs with appropriate training and under the license of the PI.
--- Monitors and evaluates patients' condition with regard to the
investigational product. --- Consults with PI regarding the
appropriate administration of investigational product. --- Conducts
routine assessments to evaluate the subject's response to
investigational product, and communicates observations to the PI,
sponsor and IRB as appropriate. --- Educates the subject about the
applicable study particulars. --- Informs/updates the subject about
pertinent study details as needed. --- Documents subject
information as it pertains to the clinical study according to the
principals of ALCOA (Attributable, Legible, Contemporaneous,
Original, Accurate). --- Meets with the study monitor to review,
verify and correct all data entered onto the case report form and
to ensure appropriate maintenance of study records. --- Reviews all
lab/tests with the physician in a timely manner. --- Reports
subject's progress, complaints and issues to PI, study sponsor, or
IRB as needed in a timely manner. --- Conducts ongoing assessments
of the overall study execution within the facility/practice,
communicating concerns to the Director, PI, study sponsor or IRB as
needed. --- Notifies appropriate management and external parties of
serious adverse events according to protocol. --- Collects
pre-study essential documents according to GCP and files
appropriately in the study record. --- Maintains the study file
record according to GCP. --- Maintains subject participant records
according to GCP. --- Provides a list of all study participants to
facility/practice management to avoid improper billing of lab tests
or services covered under the research budget. --- Ensures
appropriate storage, access, and maintenance of records pertaining
to investigational product. --- Documents investigational product
received dispensed, and returned to study sponsor according to GCP.
--- Completes the clinical trials management system and
electronic/paper case report forms in an accurate and timely manner
--- Attends Investigator Meetings as necessary. --- Prepares
abstracts and posters/talks for scientific conferences as required
--- Participates in preparation of manuscripts for publication in
peer-reviewed scientific journals as required --- Other duties as
assigned. PHYSICAL DEMANDS AND WORKING CONDITIONS: --- The physical
demands and work environment characteristics described here are
representative of those an employee encounters while performing the
essential functions of this job. Reasonable accommodations may be
made to enable individuals with disabilities to perform the
essential functions. --- Day to day work includes desk and personal
computer work and interaction with patients, facility staff and
physicians. --- The work environment is characteristic of a health
care facility with air temperature control and moderate noise
levels. May be exposed to infectious and contagious
diseases/materials. --- The position requires 10 - 15% travel
between assigned facilities and various locations within the
community. Travel to regional, Business Unit and Corporate meetings
may be required. SUPERVISION: --- None EDUCATION: --- Graduate of a
technical program in healthcare (e.g., LVN/LPN, Medical Assistant
or Dialysis Technician) AA in Life Sciences or other health related
field. Advanced Degree preferred. EXPERIENCE AND REQUIRED SKILLS:
--- 2 to 5 years' healthcare experience with Dialysis experience
preferred. --- Research experience preferred. --- Willing to pursue
CCRC or SoCRA certification when eligible. --- Current appropriate
state licensure if applicable. --- Proficient with PCs and
Microsoft Office applications. --- Good communication and
organizational skills. --- Ability to work independently.Talent
Burst Job ID #26889266. Pay package is based on 8 hour shifts and
40 hours per week (subject to confirmation) with tax-free stipend
amount to be determined. Posted job title: Clinical Research
CoordinatorAbout TalentBurst, IncTalentBurst Health & Life Sciences
is an established provider of healthcare workforce solutions,
servicing healthcare facilities across the United States for over
15 years. As a Joint Commission Certified Agency, our commitment to
quality, integrity, and exceptional service has made us a trusted
name in the healthcare staffing landscape.Our mission is to bridge
the gap between healthcare professionals seeking fulfilling
opportunities and healthcare organizations striving to maintain
their high standards of care. We are committed to providing
top-notch healthcare professionals with access to facilities where
they can focus on delivering exceptional patient care and
thrive.Whether you're a nurse, allied health professional, or
administrative personnel, we have the expertise to match your
skills and aspirations with the perfect placement. -
Keywords: TalentBurst, Inc, North Bergen , Travel Clinical Research Coordinator - $1,020 per week, Other , New York, New Jersey
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