Clinical Research Associate

An ever-growing CRO are looking for a Clinical Research Associate to join their highly-skilled team. This is a remote role, however, you will be expected to complete up to 6-8 site visits a month. The role comes with a competitive salary and a car allowance. The Company They are global leader in providing services in clinical trials, carried through to the highest of standards. There is a continued emphasis on the patients as they are reliant upon the advancements the team make within drug discovery. They are renowned for their commitment to their clients, ensuring all projects are carried out to budget, on time and to the highest quality. CRA Role This brilliant opportunity is about conducting visits to assess regulatory and protocol compliance and manage all the required documentation surrounding the clinical trial. Ensuring the trials are exceeding the client's expectations, by coordinating and performing all aspects of the site management and clinical monitoring process successfully. Further Responsibilities Include. Complete project activities associated with monitoring functions of Phase I-IV clinical research studies whilst developing mastery and a thorough understanding of the drug development process. Perform monitoring functions to assess the progress of clinical studies at assigned investigative sites (either on site or remotely) to ensure clinical trials are conducted, recorded. Ensure all trials are reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. CRA Requirements Previous clinical monitoring experience essential. Ability to travel 6-8 days on-site per month. Strong academic life science background. Past pharmaceutical or biotech experience - CRO preferable. . The interview process includes a telephone interview followed by a video interview. If this sounds like the role for you, please apply now If you want to discuss similar opportunities email me at

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