Clinical Trial Assistant

Clinical Trial Assistant (CTA) – Permanent – Boston, MA

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 Clinical Trial Assistant (CTA) to join our team in the US working office based in Boston. 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.

THE ROLE:

As a 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)

• Reviewing monitoring visit resports

• 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

THE CANDIDATE:

To be successful in the role of 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

• 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 Boston

   

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 medical, dental and vision cover, health reimbursement arrangement (HRA), flexible spending accounts (FSA),  401K pension plan, short and long term disability insurance and generous paid time off.

• 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 careers@clintec.com for more information!

THE COMPANY

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

KEY WORDS:

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