Independently drafts protocols, sample analysis outlines (SAOs), amendments and study schedules as appropriate, using proposal outline or client-supplied information.
Reviews study compliance against protocol, SOP, and regulatory agency guidelines.
Learns to serves as the primary contact in communication and interaction with other departments and clients as applicable.
Updates and maintains project tracking systems as appropriate.
Participates in and assists Study Director/Principal Investigator (SD/PI) with pre-initiation and other study related meetings, including scheduling and leading meetings as required.
Learns to manage increasingly complex projects and study designs and/or increased study load.
Responsible for report preparation, including table and figure preparation.
Assists in evaluating data for reports.
Maintains well documented, organized, and up-to-date study files including study schedule, protocol, and correspondence, as applicable.
Reviews QAU report audits and submits audit responses for approval as appropriate.
Reviews client comments and makes decisions, including appropriate study personnel as necessary, to ensure that all necessary report/raw data clarifications are completed.
Responsible for report production through finalization, including archival of data as appropriate.
Assists with routine client visits as requested. Manages data transfer to clients as requested.
Assists SD/PI in monitoring study phases.
Performs other related duties as assigned.

Bachelors Degree
2 or more years of experience in relevant position
Bachelors Degree in a Science field (e.g. chemistry or biology)
1 year or more experience preparing spreadsheet reports including tables
Use word processing software, database, spreadsheet, and specialized software
Excellent communication and interpersonal skills
Excellent attention to detail
Ability to prioritize, organize, and manage time

21 permanent Biotechnology / Life Sciences jobs in Leeds