Study Coordinator Bioanalysis

7 months ago

Harrogate, United Kingdom Labcorp Full time

**Are you looking for a office based scientific role?**

**Do you have excellent communication skills and attention to detail?**

**Are you looking for a role with training and career progression opportunities?**

**Do you want to be a part of the world's leading drug development company?**

At Labcorp in **Harrogate, North Yorkshire, **we are looking to recruit a **Study Coordinator to join our Bioanalysis department.**

This role is to undertake routine checking of analytical data and reports generated in Bioanalysis (LC-MS/MS). Develop an understanding of bioanalytical method validation and sample analysis. Responsible for coordinating the activities of routine and non-routine studies in a timely, efficient, and quality manner.

**Job responsibilities include**:

- Drafts protocols using study outline or client supplied information
- Prepares study protocol amendments
- coordinates with other teams to ensure the study lifecycle progresses as per standard or Client-agreed timelines
- Works with SD/PI to prepare and communicate data transfers and updates to clients throughout the in-life phase
- Aids in report preparation, including tables and figures. Compiles analytical information from laboratory groups
- Maintains well documented, organised and up-to-date study files including study schedule, protocol and correspondence
- 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
- Reviews client comments with SD/PI and ensures that all necessary report/raw data clarifications are completed
- Oversees report production through finalisation, including archiving of data.
- Participates in routine client visits under direction of the SD/PI
- Interacts/communicates with client regarding study issues
- Assists SD/PI in monitoring in-life and analytical phases of studies, if applicable and review of study compliance with Protocol, SOPs and regulations (e.g. UK/OECD GLP/GCP)

**What Labcorp can offer you**:

- Competitive salary and a comprehensive benefits package, including health coverage and contributory pension
- Ability to work with a variety of different clients on wide ranging projects
- Flexible working and career development opportunities

**Education**:

- Scientific degree (Biochemistry, Chemistry, Biology, Molecular Biology, Biomedical Sciences etc)
- ** OR** relevant scientific industry experience

**Experience**:

- Writing reports or administrative experience would be beneficial
- Skilled in concise writing, requiring little third-party review or editing
- Ability to utilize word-processing software, databases, spreadsheet and specialized software
- Knowledge of the variety of studies performed in the department
- Knowledge of GLP, GCP and guidelines, as applicable
- Responds efficiently to requests, and delivers on commitments
- Demonstrates and promotes teamwork
- Adapts well to changing situations/priorities, and overcomes obstacles
- Demonstrates good internal and external client interactions
- Strives to enhance knowledge and skills
- Responsible for notifying the SD/PI or management of any unforeseen circumstances that may affect the quality and integrity of the study. Works with the SD/PI to ensure that these items are identified, documented and corrected
- Exercises limited judgement in drafting protocols, amendments and routine reports
- Possesses detailed view of all phases of the project

**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.

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