Covance PK Coordinator I in Leeds, United Kingdom
Get ready to redefine what’s possible and discover your extraordinary potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose , you’ll be empowered to own your career journey with mentoring, training and personalized development planning.
Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.
We have a job opening for a PK Coordinator in internal Covance team, Leeds, UK! We are looking for people interested in full time options, biology and pharmacology !
The PK Coordinator will liaise with the relevant bioanalytical departments over the transfer of clinical PK and PD data.
Responsibilities associated with this position:
Maintains own schedules for CDARO PK and stand-alone PK studies
Creates and maintains PK Analysis Plan (PKAP) under the supervision of the study pharmacokineticist (Pkist) and/or group manager
Conducts non-compartmental (NCA) PK analysis in accordance with the protocol, protocol amendments and/or PKAP under guidance from the study Pkist or group manager
Prepares PK analysis methodology sections and compiles stand-alone PK report tables and figures under guidance from study Pkist or group manager
Conducts non-compartmental analysis on clinical datasets for use in interim PK reports under guidance from the study Pkist or group manager
Draft interim clinical PK reports, including Tables, Figures and Listings
Performs QC checking of analysis datasets and/or reports (text, tables and figures) for CDARO and stand-alone PK studies to ensure accuracy and completeness
Reviews QA/QC report audits and Sponsor comments for CDARO and stand-alone PK reports with the study Pkist
Responds to and incorporates QA/QC findings and Sponsor comments into the final reports under guidance from study Pkist or group manager
Proactively communicates and interacts with study team, other departments, and clients
Assists study Pkist in communication and interaction with other departments and clients, as applicable
Participates in process improvement projects to increase the efficiency of daily/routine procedures and reporting methods
Archives clinical PK data in a timely manner
Any other duties as assigned by the group manager or Associate Director
Covance believes that their best-in-class employees deserve first-class benefits. Covance offers an outstanding benefits package including medical & dental insurance, tuition reimbursement, short and long-term disability, and life insurance.
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.
Education / Qualifications
Bachelor degree in a scientific discipline
Experience may be substituted for education
Ability to learn/utilize PK software (Phoenix WinNonlin), word processing software, database, spreadsheet, and other specialized software like SigmaPlot
At least one year of general experience in relevant scientific or clinical fields
Excellent communication and interpersonal skills
Job Number 2018-20427
Job Category Clinical Operations
Position Type Full-Time
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.