• We use cookies to help make our website work. LEARN MORE

Clinical Research Associate

Manchester   •  £150 - 200 per day  •  Contract/Temporary, Full time

Clinical Research Associate role

  • 6-month contract
  • 150-200 per day
  • North West

Do you consider yourself to have effective time-management, the ability to collaborate well with others and regard yourself as an organised individual? If so, then you may be successful in this CRA role working for a highly regarded academic institute. This role is located within the North-West region, on a 6-month contract.

Responsibilities day to day may include:

-Collaborating with other CRAs, the Local Study Team and Local Study Manager to ensure that commitments of the study are achieved efficiently and in a timely manner.

-Monitoring the delivery of the study, making sure everything is conducted in a complicit way.

-Actively participating in Local Study Team (LST) meetings.

-Training, supporting and advising Investigators and site staff in study related matters.

-Updating CTMS and other systems with data from study sites as per required timelines.

-Managing study supplies (ISF, etc), drug supplies and drug accountability at study site.

-Performing Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.

-Performing regular Site Quality Risk Assessments, adapting intensity of monitoring as the study progresses.

-Ensuring accurate and timely reporting of Serious Adverse Events and their follow ups.

-Ensures that all study documents are available and ready for final archiving and completion of local part of the eTMF.

Requirements for the role:

-Batchelors degree, preferably within Life Sciences

-Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.

-Good medical knowledge and ability to learn relevant AZ Therapeutic Areas.

-Basic understanding of the drug development process.

-Good understanding of Clinical Study Management including monitoring, study drug handling and data management.

-Valid driving license

-Good analytical and problem-solving skills.

-Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.

-Familiar with risk-based monitoring approach including remote monitoring.

-Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.

-Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.

If you would like more information on this role or think you would be a great fit, please do not hesitate to get in contact via email to Alannah.White@cpl.com

  • Agency: Cpl Life Sciences
  • Contact: Alannah White
  • Reference: JO-2111-480081
  • Posted: 12th November 2021
  • Expires: 10th December 2021

Cpl Life Sciences

Share this job: