Labcorp Drug Development are helping to develop what could be the first pharmacological treatment able to help 3+ million severily ill hospitalized patients worldwide… and we need you to contribute with your expertise.

Labcorp Drug Development

With all the uncertainty in the world, your job stability should not be a concern.

But We Are Much More Than a Normal CRO

Labcorp have supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today.

• We are also the world´s biggest Central Lab, generating more clinical trial data than all other central laboratories combined
• Our Early Phase Solutions have proved to shave off 30 % time from lead candidate to Proof of Concept
• LabCorp were the first in receiving FDA approval to perform COVID19 tests using an at-home collection kit.
  

Join us and see why Labcorp Drug Development are uniquely positioned to offer you not only a job, but a stable, long-term international career, and why more than 90% of the top 20 global pharmaceutical companies are repeat customers.

APPLY NOW

The Clinical Trial Assistant (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience, and level of contribution which they can make to the project. The CTA performs study-related tasks as required by the department, including (but not limited to): communicate with project team members regarding study updates, maintain documentation as required by protocols, SOPs and regulatory standards, to ensure timely production of high quality clinical data, provide systems support, track information related to the status of study activities and assist with general administrative functions as required. Activities will be conducted in compliance with Company or Sponsor SOPs and regulatory standards and guidelines applicable.

• Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support
• Assist in the preparation of study and site specific materials in accordance with relevant SOPs
• Complete minute taking and documentation for sponsor/external or internal teleconferences as requested
• Assist in setting up and maintaining tracking systems/spreadsheet for e.g. study supplies
• Maintain the Project Directory
• Provide support for Investigator Meetings; track meeting attendees and/or other information regarding the Investigator Meeting
• Provide support to project team (e.g. proof-reading and editing correspondence, mailings, shipping of study files, faxing and photocopying documents, assembling study documents, and arranging meetings, etc.)
• Maintain Trial Master File documentation within the appropriate TMF platform, participate in TMF QC, as assigned, and track and /archive as applicable
• Audit and CAPA tracking
• Set up and maintain clinical investigator files and documentation
• Liaise with vendors, as needed, for study conduct such as printing study materials and/or external systems access for study team members.
• Coordinate and plan study supply shipments with vendors
• Maintain and confirm shipment information such as courier tracking numbers and date of shipping and delivery
• Prepare/assemble/ship supplies to sites pre-SIV: Study File Notebooks, CRFs, other study-specific ancillary supplies (i.e. diary cards, patient visit reminders);
• Generate reports as needed, for example CTMS site contact information list
• Work with the In-House CRA and other project team members on reconciliation of data with CTMS.
• General communications to sponsors, sites and internal team members via electronic mail or courier or telephone
• Perform other administrative duties as assigned by Line Manager, Project Managers or Clinical Trial Lead.
  

… so we can tell you about the cookies & brownie days, the sense of humor and team support that permeate everything we do, how our managers constantly review study/site allocation to ensure workload balance or why you will not grow a stale career with us

Labcorp Is Proud To Be An Equal Opportunity Employer

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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

Labcorp Is Proud To Be An Equal Opportunity Employer

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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

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