Covance Associate Study Coordinator - Metabolism in Harrogate, United Kingdom
COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.
We are recruiting for our Early Compound Development Unit team in Harrogate and are currently seeking to hire an Associate Study Coordinator – Metabolism to help support the metabolism-Study Direction team.
This is a full time permanent position, based in our site in Harrogate.
Essential Job Duties:
Performs initial review of analytical data and originates noncompartmental analysis in support of pharmacokinetic and toxicokinetic studies
Reviews study compliance against protocol, SOP and regulatory agency guidelines
Prepares study schedules based on input from Study Director (SD)/Principal Investigator (PI), places information into databases and communicates work plan to laboratory personnel and support groups, as applicable.
Participates in and assists SD/PI with pre-initiation and other study related meetings as required
Reviews progress and study status against initial work plan – maintains CMS with accurate schedules.
Proactively communicates and interacts with study team to ensure key milestones are achieved
Serves as the primary contact in communication and interaction with other departments and clients as applicable
Maintains well documented, organised and up-to-date study files including study schedule, protocol and correspondence.
Assists SD/PI in the PK/TK study phase, if applicable and review of study compliance with protocol, SOPs and regulatory guidelines.
Aids in report preparation, including tables and figures. Compiles analytical information from laboratory groups.
Assists in the development and maintenance of standard report/table formats as required
Assists in interpreting and evaluating data for reports
Participates in the peer review process for scientific reports
Reviews QAU report audits with SD/PI or appropriate laboratory group. Submits audit responses for SD/PI approval. Ensures that all necessary report/raw data clarifications are completed.
Learns to deputise for SD in their absence with ability to provide updates to internal/external customers
Reviews client comments and makes decisions in conjunction with SD/PI and ensures that all necessary report/raw data clarifications are completed.
Regularly manages increasingly more complex projects and study designs and/or increased study load
Responsible for and drives report production through finalization, including archiving of data as appropriate.
Prepares for and participates in routine client visits under direction of the SD/PI. Hosts routine client visits and interacts/communicates with client as necessary.
Maintains an awareness of the financial status of ongoing studies, including work scope changes
Develops an area of expertise within the department and serves as a resource by providing training an written instructions
Develops knowledge of Covance metabolism capabilities such that they can coordinate (with supervision) one other area outside of their area of expertise
Learns to expand responsibilities as a project coordinator for assigned clients(s) across the metabolism discipline
Performs other related duties as assigned.
Education / Qualifications
Relevant degree plus 2 years of appropriate experience. Relevant experience may be substituted for academic qualifications.
Ability to utilise word processing, databases, spreadsheets, and specialised software on personal computers.
- Skilled in the use of all standard laboratory equipment
Job Number 2018-19318
Job Category Scientific Entry Level
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.