Clinical Scientist, Clinical Science Rare Genetic and Hematology (RGH) Therapeutic Area
Company: Takeda Pharmaceutical
Location: Montvale
Posted on: May 13, 2022
|
|
Job Description:
By clicking the "Apply" button, I understand that my employment
application process with Takeda will commence and that the
information I provide in my application will be processed in line
with Takeda's Privacy Notice and Terms of Use . I further attest
that all information I submit in my employment application is true
to the best of my knowledge.
Job Description
Are you looking for a patient-focused, innovation-driven company
that will inspire you and empower you to shine? Join us as a
Clinical Scientist, Clinical Science RGH, in our Cambridge, MA
office.
At Takeda, we are transforming the pharmaceutical industry through
our R&D-driven market leadership and being a values-led
company. To do this, we empower our people to realize their
potential through life-changing work. Certified as a Global Top
Employer, we offer stimulating careers, encourage innovation, and
strive for excellence in everything we do. We foster an inclusive,
collaborative workplace, in which our global teams are united by an
unwavering commitment to deliver Better Health and a Brighter
Future to people around the world.
Here, you will be a vital contributor to our inspiring, bold
mission.
POSITION OBJECTIVES:
Responsible for providing scientific support for the company's
clinical research and product development initiatives under the
direction of GCDL
POSITION ACCOUNTABILITIES:
Provides clinical scientist input into regulatory questions, runs
ad hoc searches Assist in the data review of patient profiles and
develop site queries as needed Summarize information relevant for
various clinical documents preparation. Assist the Medical Monitor
(CDL) in the review of trial data and development and review of
clinical study documents, reports etc, Serve as a resource to
address medical questions or clarify issues arising during conduct
of the study Support CDL to provide scientific leadership in
execution of clinical trials Provide relevant clinical scientist
expertise to internal teams, including clinical operations, medical
writing, data management, pharmacovigilance to ensure quality
processes and deliverables Assist with ongoing monitoring of safety
data and participates in drug safety surveillance for Development
projects Collaborates with CDL, and Global Product Team Lead, to
ensure that all development and product support activities for the
assigned projects are coordinated and consistent. Interacts as
needed with Clinical Development partners such as Clinical
Operations, Regulatory, Commercial, Compliance, and Business Unit
management teams. Supports the CDL when participating in
clinical/medical advisory panels, steering committees and
investigator meetings. Remains up-to-date with current information
on pharmaceutical regulations, guidelines, and practices and
therapeutic area knowledge and ensures consistent best practice
across all activities. Assists in the development of clinical
studies and reviews clinical protocols and clinical study reports
for scientific and operational accuracy.
EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:
MD/PharmD/PhD required Minimum 2+ years) in clinical research
within the pharmaceutical industry CRO or similar organization.
Demonstrated ability to collaborate in a matrixed environment
Experience in submissions of IND/CTA/NDA/MAA and interactions with
Regulatory authorities Experience in designing and conducting
clinical trials; and/or significant late-stage development
research. Experience in rare diseases a plus Able to work
independently, prioritize and meet project timelines Able to
effectively present information Demonstrated ability to work
cooperatively within and outside the organization to accomplish the
best outcomes; ability to build and support teams of diverse
backgrounds Good analytical skills and ability to review emerging
data and clinical outputs are required in order to make appropriate
decisions and institute measures to ensure quality results and
safety. It is expected that incumbent will take initiative and work
independently, however, ongoing communication with CDL is a vital
part of problem-solving and decision-making.
Absent an approved religious or medical reason, all US office-based
and lab-based Takeda employees who work fully on-site or in a
hybrid model (as determined by Takeda) must be fully vaccinated to
work at a Takeda site or to engage with Takeda colleagues or anyone
else on behalf of Takeda. US field-based employees must be fully
vaccinated as a condition of employment, absent an approved
religious or medical reason. US employees who work at a Takeda
manufacturing facility, and those who work at a BioLife center or
BioLife lab, may be subject to different guidelines. If you are
contacted by a Takeda recruiter about your job application, we
encourage you to seek more information on the applicable guidelines
for the Business Unit/Function to which you have applied.
In accordance with the CO Equal Pay Act, Colorado Applicants Are
Not Permitted to Apply.
WHAT TAKEDA CAN OFFER YOU:
401(k) with company match and Annual Retirement Contribution Plan
Tuition reimbursement Company match of charitable contributions
Health & Wellness programs including onsite flu shots and health
screenings Generous time off for vacation and the option to
purchase additional vacation days Community Outreach Programs
Empowering Our People to Shine
Discover more at takedajobs.com
No Phone Calls or Recruiters Please.
#LI-JV2
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce
and providing equal employment opportunities to all employees and
applicants for employment without regard to race, color, religion,
sex, sexual orientation, gender identity, gender expression,
parental status, national origin, age, disability, citizenship
status, genetic information or characteristics, marital status,
status as a Vietnam era veteran, special disabled veteran, or other
protected veteran in accordance with applicable federal, state and
local laws, and any other characteristic protected by law.
Locations
Boston, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Keywords: Takeda Pharmaceutical, Yonkers , Clinical Scientist, Clinical Science Rare Genetic and Hematology (RGH) Therapeutic Area, Healthcare , Montvale, New York
Click
here to apply!
|