Clinical Project Scientist, Oncology
Company: Disability Solutions
Location: Spring House
Posted on: April 20, 2024
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Job Description:
At Johnson & Johnson, we believe health is everything. Our
strength in healthcare innovation empowers us to build a world
where complex diseases are prevented, treated, and cured, where
treatments are smarter and less invasive, and solutions are
personal. Through our expertise in Innovative Medicine and MedTech,
we are uniquely positioned to innovate across the full spectrum of
healthcare solutions today to deliver the breakthroughs of
tomorrow, and profoundly impact health for humanity. Learn more at
. Johnson & Johnson is recruiting for a Clinical Project Scientist,
Oncology. The position can be located in Spring House, PA; Raritan,
NJ; High Wycombe, UK; Beerse, Belgium; Breda, Netherlands; or
Issy-les-Moulineaux, France. Remote work options within the United
States, United Kingdom and European Union may be considered on a
case-by-case basis and if approved by the company. The Clinical
Project Scientist (CPS) works in the Oncology Therapeutic Area
Development group, and participates in the development, oversight,
and execution of Ph I-IV clinical research trials working closely
with Study Responsible Physicians and other Clinical Project
Scientists. The position reports to a more senior Clinical Project
Scientist. Primary Responsibilities Include: --- For ongoing
clinical trials, this individual in collaboration with the Study
Responsible Physician/other Clinical Project Scientists, will
participate in or lead aspects of aggregate and participant level
data, including patient screening/eligibility evaluation, PK/PD
data, adverse events, efficacy, coding, and other data critical to
study endpoints --- May participate in drafting protocol synopses,
sections of full protocols, informed consent documents, and will
review Case Report Forms (CRFs) and other data collection tools
against draft protocols and central vendor scope of work --- May
partner with the lead CPS/Cross Functional Trial Team to mitigate
issues in initiation of clinical trials and may participate in
review of Monitoring Guidelines, SET/IDMC Charter, Statistical
Analysis Plan, Data Management, and Safety Management Plans --- May
perform medical monitoring/reporting, evaluates ongoing clinical
trial data --- May partner with the lead CPS drafting Medical
Review Plan and Medical Review Forms --- May liaise with vendor
laboratories, Translational Research lead, pharmacokinetic
operations and/or biomarker operations to ensure sample collection,
processing, and tracking --- May liaise with Integrated Data
Analysis & Reporting team in set-up of data visualization tools
(e.g., iDARTs) --- May participate in or lead aspects of training
the central study team, local study team, site personnel or
external vendors on protocol, disease evaluation criteria, or other
specific aspects of the clinical study --- May participate in data
review and drafting documents for Health Care Authority
interactions. --- Will actively participate in mentorship and
training opportunities to expand clinical development knowledge,
therapeutic area expertise, and leadership capabilities
Keywords: Disability Solutions, Cherry Hill , Clinical Project Scientist, Oncology, Healthcare , Spring House, New Jersey
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