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provide a culture in which our employees can enjoy personal
satisfaction, professional achievement and have the ability to
strategically map out long-term career plans. If you're ready to be
a part of something inspiring join us and Discover Your PRA.
Who are we?
We Are PRA.
We are 16,000+ employees strong, operating in more than 90+
countries. We are committed to saving lives and we are constantly
striving to be the best at what we do. Our impact is real and we
see it every single day. We help get life-saving drugs into the
hands of those who need them most.
What will you be doing?
Joining a well-established yet expanding team fully outsourced
to one of our global pharmaceutical clients, the Clinical Trial
Manager ensures overall successful execution of phase 1-4 clinical
trials in multiple therapeutic areas, in accordance with applicable
Standard Operating Procedures, agreed timelines, budgetary and
regulatory requirements, at a global scale.
The Clinical Trial Manager serves as the leader for the Study
Management Team, with ultimate responsibility for the set-up,
planning and coordination of clinical trials through to study
closure. Managing and tracking key study metrics to ensure
adherence to project milestones, along with communicating with
other departments, will form a key part of this role.
Reporting to a Clinical Program Leader, you will ensure accurate
budget management, including guaranteeing that third-party vendors
are working to defined plans.
Other fundamental tasks include driving activity to ensure that
enrolment commitments are met, whilst also checking that relevant
documentation is duly updated, resolving problems, proactively
managing risk and (where necessary) timely escalating issues.
Clearly, the Clinical Trial Manager will also work in accordance
with applicable health authority regulations and internal standard
operating procedures. Where necessary, participation in the
preparation for and conduct of Health Authority inspections and
internal audits will also feature in this role.
Working at the very heart of the clinical trial, you will
deliver appropriate training to your study team on a trial-specific
basis. Additionally, you will act as a key liaison with Quality
Management in order to establish a high level of quality throughout
the project lifecycle.
The successful candidate will be an expert study manager, will
have a proven record of successful execution of clinical trials on
a global study. You will be able to work to key metrics and
motivate a regionally-based study team throughout the project
lifecycle. Your experience in the set-up and management of
third-party vendors, as well as global study start up, will be
self-evident. Familiarity with phase 1-4 studies would be highly
advantageous. Demonstrable knowledge of effective project planning,
strong financial acumen, along with the flexibility to manage a
virtual team will ensure success within this position.
Previous experience of working with multiple therapeutic areas,
including cardiology/metabolism, infectious disease, immunology
and/or vaccines is preferred.
Candidates from either a pharmaceutical or CRO background are
welcome to apply.
BS degree or equivalent required, preferably in Life Sciences
(e.g., Biology, Chemistry, Biochemistry, Nursing, and
Minimum of 6 years clinical trial management experience in the
pharmaceutical industry or CRO, however, other relevant experiences
and skills may be considered by the hiring manager when considering
the candidate's eligibility.
Willing to travel up to 20%
- To qualify, applicants must be legally authorized to work in
the United States or Canada, and should not require, now or in the
future, sponsorship for employment visa status.
PRA is an EEO/AA employer and is committed to providing
opportunities to minorities, women, veterans and individuals with