Clinical Lead, Multiple Therapeutic Areas
Company: IQVIA Argentina
Location: Dallas
Posted on: February 25, 2021
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Job Description:
Help create a
healthier world. Start right here at IQVIA. Clinical Lead, Multiple
Therapeutic Areas Locations: Boston, MA,USA;Cambridge, MA (USCBG1,
40, H),USA;Charlotte, NC,USA;Charlottesville, VA,USA;Chicago,
IL,USA;Dallas, TX,USA;Houston, TX,USA;Los Angeles, CA,USA;Miami,
FL,USA;Minneapolis, MN,USA;Orlando, FL,USA;Parsippany, NJ (USPAR1,
40),USA;Philadelphia, PA,USA;Phoenix, AZ,USA;Piscataway,
NJ,USA;Salt Lake City, UT,USA;San Diego, CA,USA;San Francisco ,
CA,USA;Trenton, NJ,USA Full time R1139183 Date Posted: 07/29/2020
PURPOSE Member of the core project team and partners with the
Project Leader to ensure overall project meets delivery
requirements. Responsible for running studies, with Lead Clinical
Analyst (LCA) support, and manage the operational aspects of
projects to meet contractual requirements and in accordance with
SOPs, policies and practices. Represent clinical delivery with
customer. RESPONSIBILITIES Manage the operational aspects of
projects to support right subjects and right data to meet or
contractual requirements. Collaborate with project leader and LCA
to establish an integrated set of plans with Clinical Lead (CL) to
be ultimately accountable for results of the clinical team.
Represent clinical delivery with customer. Produce and distribute
status, tracking and financial reports for the core project team,
other functional groups and senior management. Responsible for
tracking financial deliverables, reporting and invoicing on
projects. Ensure appropriate subject recruitment plans are in
place; all outreach or digital offerings are explored and deployed
in consultation with the customer. Ensure the Site Recruitment
Action Plan (SRAP), patient recruitment target and contingency
plans are in place and deployed at trigger points. Deliver the
project / program according to the quality management plan. Guide
CRAs and advise on critical specific study issues. Manage clinical
study set-up, maintenance and follow-up study activities through
ongoing tracking and review of study progress. Report progress to
appropriate clinical management and project management forums.
Accountable for approving final sites lists. Develop the risk
management plan from a clinical perspective and coordinate clinical
issue escalation and resolution with the Project Leader.
Collaborate with other functional groups such as Global Delivery
Network (GDN), Labs, Data Management, Pharmacovigilence, and
Biostatistics, where necessary, to support milestone achievement
and to manage study issues and obstacles. Provide ongoing training
and support to the clinical team. Conduct frequent team meetings
and ensure regular communication. Drive high performance and
efficiency of the clinical team through CRA project objectives, the
conduct of monitoring visits. Provide performance feedback to
management on clinical team members. Utilize appropriate clinical
tools, processes and GDN for the study team to support the
execution of clinical deliverable and study timelines. REQUIRED
KNOWLEDGE, SKILLS AND ABILITIES Good knowledge of Clinical Practice
(GCP) and International Conference on Harmonization (ICH)
guidelines Proven ability to work through others to deliver results
to the appropriate quality and timeline metrics Proven ability to
understand customer needs and appropriately influence decision
making Effective mentoring and training skills Ability to balance
operational and strategic priorities Strong communication and
interpersonal skills, including good command of English language
Demonstrated proficiency in using systems and technology to achieve
work objectives Demonstrated proficiency at analyzing data and
information to make conclusions and drive sound decision making
MINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor's degree in a
health care or other scientific discipline with 5 years clinical
research/monitoring experience; or equivalent combination of
education, training and experience. PHYSICAL REQUIREMENTS Extensive
use of telephone and face-to-face communication requiring accurate
perception of speech Extensive use of keyboard requiring repetitive
motion of fingers Regular sitting for extended periods of time
#c1920 At IQVIA, we believe in pushing the boundaries of human
science and data science to make the biggest impact possible - to
help our customers create a healthier world. The advanced
analytics, technology solutions and contract research services we
provide to the life sciences industry are made possible by our
67,000+ employees around the world who apply their insight,
curiosity and intellectual courage every step of the way. Learn
more at jobs.iqvia.com .
IQVIA is an EEO Employer - Minorities/Females/Protected
Veterans/Disabled IQVIA, Inc. provides reasonable accommodations
for applicants with disabilities. Applicants who require reasonable
accommodation to submit an application for employment or otherwise
participate in the application process should contact IQVIA's
Talent Acquisition team at workday_recruiting@iqvia.com to arrange
for such an accommodation.
Keywords: IQVIA Argentina, Dallas , Clinical Lead, Multiple Therapeutic Areas, Healthcare , Dallas, Texas
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