Senior Clinical Trial Assistant (SCTA) - Office Based - Raleigh, NC
Do you want to be part of an award-winning global clinical research organisation who is positively working towards improving the health and lives of millions?
Clintec are currently hiring for a Senior Clinical Trial Assistant (CTA) to join our team in the US working office based in Raleigh. If you are looking for an opportunity to work with a dynamic, forward-thinking CRO with real career development opportunities then we would love to hear from you.
As a Senior Clinical Trial Assistant (CTA) you will support trial and site administration, manage documents and support with regulatory and start up activities. Responsibilities include:
Tracking and reporting of essential documents
Updating clinical trial systems and databases (CTMS)
Collating, archiving and distributing study documents (TMF)
Updating study materials (e.g. Patient diaries, instructions)
Updating investigator lists for site evaluation and start up
Preparing packages for submissions to Regulatory authorities and Ethical committees
Working closely with finance teams for tracking and reporting of budget negotiations, contract development and management of investigator and site payments
Organising and supporting meetings, including investigator meetings
To be successful in the role of Senior Clinical Trial Assistant (CTA) candidates should have:
Previous experience working within Clinical Trials in a similar role
Degree level education, ideally within Life Science’s / Healthcare
Fluency in English language (written and spoken)
Strong organisational and communication skills
Ability to work with a wide range of people
Basic knowledge of accounting and financial procedures
Willing and able to work office based in NC
WHAT’S IN IT FOR YOU?
At Clintec, we understand that our people are our biggest asset and we value the hard work and dedication of all our employees.
By joining the Clintec team you can expect:
Competitive salary and benefits packages for permanent employees including country specific benefits such as:
20 days annual leave plus 10 days annual public holidays, health/vision/dental care plus short/long term disability cover, retirement savings and group life assurance
Opportunity to work with global pharmaceutical leaders in roles fully dedicated to a single sponsor
Opportunity to work on ground-breaking, challenging studies in various therapeutic areas
Real career development opportunities within a friendly and social team where you can truly shine and make an impact
Click Apply Now to send your CV of email us directly on firstname.lastname@example.org for more information!
Clintec (an IQVIA company), established for 22 years, is an award-winning, full-service global clinical research organisation with our HQ office based in Scotland, UK. We support key product development and manage clinical trials in over 50 countries worldwide, across all major therapeutic areas, with expertise in Oncology and Rare Disease studies. We differ from other players in the clinical research industry as we combine the agility and flexibility typical of smaller CROs with the global coverage and management associated with large CROs.
Find out more by visiting www.clintec.com
CTA / Clinical Trial Assistant / Clinical Trial Administrator / Study Start-up / Clinical Trial Coordinator / CRC / Clinical Trial Coordination / Clinical Trials Administration / Clinical Research Coordinator / Clinical Project Associate / Oncology / Pharmaceutical Industry / Clinical Site Relationship / patients trackers / TMF / CTMS / submissions