As an Associate Data Coordinator, Premier Research is looking for driven individuals to join our Clinical Data Sciences team. This position may be your ticket to turning innovative concepts into ground-breaking treatments, equipment, and diagnostics if you’re hoping to have a big influence in the biotech, medtech, and specialized pharmaceutical industries.
Our work at Premier Research is closely related to enhancing and saving lives. We assist cutting-edge biotech and specialty pharmaceutical firms in launching novel therapies. Our team members are empowered when we provide them with the freedom, well-being, and chances to develop both personally and professionally.
Job Responsibilities
In our data management procedures, you will be an essential member of the team as an Associate Data Coordinator. Your primary duties will consist of:
- helping to prepare documentation, including data report specifications, external data transfer specifications, data management plans (DMPs), and clinical case report guidelines (CCGs).
- supporting testing edit checks as part of User Acceptance Testing (UAT) on studies.
- facilitating database upgrades and helping to maintain databases.
- creating reports in order to examine data.
- checking data listings and Case Report Forms (CRFs) to make sure all data is collected in accordance with the DMP, CCGs, and protocol.
- creating and examining queries, addressing any inconsistencies that surface.
Qualifications and Skills
We are seeking applicants who fulfill the subsequent requirements:
- Education: a bachelor’s degree or above, ideally in the B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences
- Experience: Ideally, you have 0–1 year of experience in the business.
- Skills: Excellent analytical abilities, a keen eye for detail, and the capacity to cooperate in a group setting.
To Apply: Apply Here
