Senior Clinical Research Associate - Oncology Experience Required - UK (North/Midlands) - FSP

Parexel International; United Kingdom; Remote; GBP 35,000 - 55,000; Full time

Job summary

Parexel International is seeking a Clinical Research Associate dedicated to oncology studies. The role involves site management, monitoring, and mentoring junior staff, while utilizing advanced technologies. This position offers job security with opportunities for career growth in a supportive environment.

Qualifications

• Experience in monitoring oncology clinical trials required.
• Ability to manage multiple tasks and prioritize effectively.
• Good understanding of phases of clinical trials.

Responsibilities

• Responsible for site management and monitoring activities across oncology studies.
• Mentor junior CRAs and collaborate with industry leaders.
• Utilize world-class technology in a pivotal role for drug development.

Skills

Time Management

Organizational Skills

Interpersonal Skills

Problem Solving

Education

Substantial Site Management experience

Understanding of clinical trial methodology and terminology

Knowledge of GCP/ICH guidelines

Job description

Parexel is currently seeking Clinical Research Associates with at least 12 months recent oncology experience to join our team and be dedicated to a single sponsor.

Working as a Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.

Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.

Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

Some specifics about this advertised role

• Dedicated to one client.

• Responsible for all site management and monitoring activities across assigned oncology studies

• Work with industry leaders and subject matter experts.

• Opportunity to mentor junior CRAs.

• Work with world-class technology.

• a pivotal role in the drug development process.

Here are a few requirements specific to this advertised role.

• Substantial Site Management experience, with an understanding of the clinical

• trial methodology and terminology.

• Experience in, or willingness to monitor oncology clinical trials.

• Experience in independent monitoring, all types of visits.

• Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.

• Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

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