A career opportunity within clinical research is a rewarding way to put your degree in life science, healthcare, maths, or statistics to work. Associates will be part of a team that have an integral role in the research and development of drugs, treatments and medical devices. Medpace is a leading, global, full-service Clinical Research Organisation (CRO) and we are looking to hire outstanding individuals for exciting careers in research to contribute to our continued success and bringing cutting edge new drugs to patients.
Following the success of our first Open Evening in London in November 2019, we are now holding another Open Evening event which will take place on Wednesday 25th March 2020 at 5:00 - 7:30 pm in our office in central London. We are inviting recent Life Sciences MSc., PhD, Pharm D graduates to learn more about industry and the various career opportunities that Medpace can offer.
Medpace UK is growing and we are currently recruiting for some of these Entry-level roles:
Project Coordinator (PC)• Provide administration support to the Clinical Trial Manager to coordinate daily project activities. Activities include meeting coordination, minutes and logistics• Point of contact for internal and external team members• Create and maintain MS project timeline and critical assessment• Pivotal to the study’s success and coordination & option for fast track to Clinical Trial Manager
Clinical Research Associate (CRA)• Comprehensive training programme that will provide you the resources and knowledge to monitor clinical sites independently• National travel 60-80% of the time - mandatory• Communicates with medical staff, clinical research physicians & internal project team• Work with world class research sites and the forefront of research
Data Coordinator • Perform QC audits of the clinical database• Reconcile clinical data and update the clinical database• Track case report forms
Regulatory Submissions Coordinator (RSC)• Assist with the start-up of clinical research sites• Prepare regulatory documents for submission to MHRA and Ethics Committees
• Prepare Informed Consent Forms• Tracks submission and site activation timelines, close coordination with project team and CRAs• Success of the trials and experimental medications reaching patients is dependent on efficient start up.
Contract Specialist
• Part of the start up team working with the RSC, negotiate project site contract language and budget directly with clinical research sites• Track, follow up on, and report on the status of documents relating to study contracts and budgets• Ensure contract and budget timelines are met • A key role in advancing the start-up of our projects
Clinical Safety Coordinator
• Responsible for the distribution of safety reports to regulatory authorities
• Create and maintain project-related trackers and status reports
• Distribute and track safety-related notifications
• Conduct quality control reviews of departmental documents.
If you have completed your degree in Life Sciences and would like to explore the career opportunities at Medpace, please send us your CV by 6th March 2020. Shortlisted candidates will be contacted with an invitation to attend the Open Evening Event.
Awards
In 2018 Medpace was recognised as a top workplace, below are a few reasons why:• Competitive compensation and benefits programmes (private medical and dental cover, eye care, pension scheme, 25 days annual leave, etc.)• Challenging, gratifying work• Extensive career development opportunities• Free on site Gym and swimming pool
About Medpace
Medpace, Inc., a clinical research organization, provides clinical development services for pharmaceutical and biotechnology
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