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Senior Clinical Research Associate

Parexel International

United Kingdom

Remote

GBP 60,000 - 80,000

7 days ago

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An established industry player is seeking a Senior Clinical Research Associate to oversee clinical site monitoring across the UK. This pivotal role demands a professional with a strong background in clinical trials, particularly in oncology and hematology. You will be the vital link between in-house teams and clinical sites, ensuring that all monitoring activities comply with the highest regulatory standards. Your expertise in GCP and CFR will be essential as you conduct site visits, provide training, and foster long-term relationships with investigative sites. Join a team that prioritizes patient well-being and contributes to groundbreaking clinical research.

At least 2 years of pharmaceutical/biotech experience required.
Prior monitoring experience and oncology/hematology trial experience essential.

Monitor and manage clinical sites, ensuring compliance with regulations.
Act as a liaison between in-house teams and clinical sites.

Clinical Monitoring

Oncology/Hematology Knowledge

Patient Well-being Focus

Communication Skills

BA/BS or equivalent

Relevant experience and training

Microsoft Office (Word, Excel, PowerPoint, SharePoint)

CTMS

EDC

eTMF

Parexel are currently recruiting for a Senior Clinical Research Associate, to cover UK sites.

In this role, the Senior Clinical Research Associate is responsible for field monitoring and management of clinical sites. This position focuses on all activities required to evaluate, initiate, monitor and close clinical sites in compliance with the Code of Federal Regulations and ICH/GCP Guidelines. This role may provide operational input to clinical study teams as directed.

Some specifics about this advertised role

Act as liaison between the in-house team, vendors, and multiple clinical sites.
Work collaboratively with investigative sites to develop strong, long-term, working relationships.
Apply SOPs, Clinical Monitoring Plan (CMP), study manuals and other materials and guidelines as applicable.
Help identify and qualify potential investigators. Perform Pre-Study Site Visits.
Assist with start-up activities, including essential document review and collection as requested.
Perform Site Initiation Visits.
Provide initial and ongoing training to site personnel regarding the study protocol, applicable policies/procedures, and GCP.
Perform Interim Monitoring Visits for assigned studies.

What we are looking for in this role

For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to us is working with heart.

Here are a few requirements specific to this advertised role.

BA/BS, or equivalent, or relevant experience and training with at least years of pharmaceutical/biotech experience. RN or health care professional preferred.
Prior monitoring experience is required. Oncology/hematology clinical trial experience is essential.
FDA/EMA inspection experience is preferred.
Proficiency in CFR and GCP/ICH Guidelines is required. Experience working on global clinical trials is preferred.
Proficiency in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint) and other electronic systems (CTMS, EDC and eTMF).

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