Clinical Trial Associate

SUMMARY

An amazing opportunity to join the leading Medical Devices organisation in Europe, to support their project managers and CRAs on clinical trials, an excellent chance to learn, develop and grow your career!

QUALIFICATIONS

•         Bachelor’s Degree

•         Experience working on clinical trials and/or clinical studies

•         Strong organization and communication skills

•         Ability to work in a matrix organization

•         Fluent in English, both in writing and speaking

•         Affinity to work with several operational systems

•         Ability to work independently in a remote environment while building relationships with your team

RESPONSIBILITIES

• Creating and managing the clinical study files and overseeing the organization and distribution of clinical study documents
• Tracking and filing Ethics Committees/Competent Authority submissions, study reports, and study documentation based on protocol requirements
• Providing technical support, which may include data extraction to compile general and customized reports, data review and tracking
• Working with various clinical IT programs, including Oracle Clinical Remote Data Capture (RDC), Siebel Clinical Trial Management System (CTSM), RAD and obtaining a broad practical knowledge of the operational systems.
• Communicating with internal and external contacts
• Assisting with periodic audits of clinical study files for completeness and accuracy
• Constantly seeking to improve processes, solve problems and improve effectiveness of job areas
• Assisting in the development, implementation and administration of program/system guidelines and procedures
• Building experience and become the right hand of the Clinical Research Specialists by, for example, helping them solve open action items, sending out study updates, completing site compliance emails/scorecards, preparing upcoming payment rounds and following up on new trainings to be sent out for study team and site personnel

SALARY

This role offers a competitive salary, please get in touch to find out more.

LOCATION

This role is based in the United Kingdom.

ABOUT PLANET PHARMA

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

www.planet-pharma.com

TO APPLY

Please click ‘apply’ or contact Kenny Brownlee at Planet Pharma for more information:

E: KBrownlee@planet-pharma.co.uk

T: +44(0)118 315 0258