Clinical Research Associate III -Senior Oncology
Company: WuXi AppTec
Location: Plainsboro
Posted on: September 8, 2023
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Job Description:
**Overview**The Clinical Research Associate III Senior Oncology
performs and coordinates aspects of field-based and office-based
monitoring and data quality control functions in accordance with
Good Clinical Practices (GCP), International Conference on
Harmonization (ICH), and WuXi Clinical Standard Operating
Procedures (SOPs). This is an office or remote based position and
requires approximately 50-75% travel.**You are applying to be part
of the WuXi Apptec Talent Pool.** We are not currently recruiting
for this role but we are building a pipeline for future
opportunities. If you would like to be considered for a similar
position in future, then please submit your
CV.**Responsibilities****Essential Job Functions:**+ Responsible
for all aspects of clinical monitoring and required reporting,
including pre-study visits, site invitation visits, routine
monitoring visits (both onsite and remote), and close-out visits.+
Completes all monitor and sponsor queries in a timely manner and
tracks and resolves protocol deviations and action items.+
Maintains awareness of current developments in Phase I - III
oncology studies relative to assigned projects.+ Trains and manages
site staff personnel on protocol requirements and other related
study items.+ Produces and maintains documentation of activities
and findings as required by WuXi Clinical and sponsor.+ Performs
data quality control functions, including but not limited to query
management and data audit functions.+ Performs other
project-related duties as specified by project manager or
supervisor, including but not limited to mentoring of Clinical
Research Associate (CRA) I and II personnel.+ Participates in team
and sponsor meetings and training programs.+ Responsible for fiscal
management of trip costs, positive feedback from site staff, low
data error rates, complete and timely site monitoring, and expense
and timesheet reporting.+ Responsible for assisting with
negotiating site budgets and contracts.+ Manages budget constraints
for travel time, time spent in-house and at site, and to manage
those constraints and to alert supervisor and project manager if
they cannot be effectively managed.+ Reviews documents in advance
of Quality Assurance review with high-level of accuracy and make
decisions on the quality of the documents and takes appropriate
action.+ Collects and reviews site regulatory documents for
accuracy and completion. Maintains study Trial Master
File/Investigator Site File.+ Solves problems independently and
anticipates risks to the project within the scope of the position
and proposes solutions to supervisor.+ Works under minimal
supervision with oversight from supervisor, project managers, and
data managers.+ Performs job specific tasks in compliance with
applicable Regulations, International Standards, and WuXi AppTec
Policies and Standard Operating Procedures.+ Assists in the
development of patient recruitment strategies.+ Monitors and
manages investigational supplies and products+ Required to perform
other duties as assigned, including assisting in other departments
as required.**Qualifications****Experience / Education:**+
Bachelor's degree required.+ Minimum of 6 years of independent
monitoring experience having completed all four visit types or
equivalent, with a minimum of 5 of these years being oncology-based
monitoring experience.+ Experience using Good Clinical Practices
and a good working knowledge of physician care in hospitals,
clinics, or other healthcare settings.+ Candidate must have
sufficient experience to be CCRA eligible.+ CCRC, CCRA, and CCRP
certifications preferred.**Knowledge / Skills / Abilities:**+ Must
have strong attention to detail and demonstrate understanding of
the critical nature of WuXi Clinical documentation.+ Must have
ability to initiate steps according to established processes
without intervention+ Must have ability to interact with internal
and external customers and sites professionally.+ Must have
excellent verbal and written communications skills in English and
concise technical writing skills with minimal grammatical or
logical errors. Ability to connect and effectively communicate with
people from various backgrounds.+ Ability to organize workload and
handle multiple priorities.+ Ability to work in a team environment
and independently while effectively managing multiple priorities
within established time constraints.+ Must possess a thorough
understanding of FDA Guidelines, ICH, GCP, NDA, IND, and other
applicable regulations.+ Ability to work in satellite environment
independently but remain engaged with home office and supervisor.+
Proficiency with Microsoft Office Suite applications.+ 50 - 75%
travel is required. Travel is primarily domestic and infrequently
international. Daily and overnight travel are required.+ Must have
a valid driver's license and the ability to rent a vehicle as
required.**Physical Requirements:**+ Must be able to work in an
office or medical site.+ Ability to stand or sit for most of the
work day.+ Must be able to perform some activities with repetitive
motion, such as keyboarding.+ Must be able to travel in various
methods of transportation (i.e., car, airplane, shuttle bus,
etc.).+ Must be able to navigate to and from site locations, hotel,
and airports with personal luggage and laptop.+ If working
remotely, must have access to high-speed internet service and have
knowledge and ability to resolve IT and computer related challenges
through remote communications channels.This job description does
not state or imply that the above are the only duties and
responsibilities assigned to this position. Employees holding this
position will be required to perform any other job-related duties
as requested by Management.WuXi AppTec requires all employees, both
Field and Office-based, to be fully vaccinated with a COVID-19
vaccine by February 9, 2022 or undergo weekly COVID-19 testing as
set forth in WuXi AppTec's Mandatory COVID-19 Vaccination Policy,
unless they are eligible for an exemption from the vaccination or
testing requirements based on a disability or sincerely held
religious belief, practice or observance. You will be required to
provide acceptable proof of your COVID-19 vaccine (if applicable)
no later than 8 days before your first day of employment.**An Equal
Opportunity Employer. All qualified applicants will receive
consideration for employment without regard to race, color,
religion, sex, sexual orientation, gender identity, national
origin, or protected veteran status and will not be discriminated
against on the basis of disability.****Need help finding the right
job?**We can recommend jobs specifically for you!An Equal
Opportunity Employer. All qualified applicants will receive
consideration for employment without regard to race, color,
religion, sex, sexual orientation, gender identity, national
origin, or protected veteran status and will not be discriminated
against on the basis of disabilityAn Equal Opportunity Employer.
All qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, national origin, or protected veteran status and
will not be discriminated against on the basis of disability
(https://careers-wuxiapptec.icims.com/connect?back=intro&findajob=1&in\_iframe=1&hashed=-435740542)**Job
Locations** _US - US_**Job ID** _2023-11600_
Keywords: WuXi AppTec, Trenton , Clinical Research Associate III -Senior Oncology, Healthcare , Plainsboro, New Jersey
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