Offer summary

Qualifications:

Extensive experience in site management and oncology trials (at least 3 years)., Minimum 3 years’ experience in independent supervision of clinical visits., Strong organizational, interpersonal, and problem-solving skills., Good understanding of clinical research, GCP/ICH guidelines, and clinical trial phases..

Key responsabilities:

Manage all site management and supervisory activities for assigned oncology studies.

Mentor junior Clinical Research Associates (CRAs).

Utilize world-class technology to support clinical studies.

Engage with industry leaders and subject matter experts in the drug development process.

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

External Job Description

If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then Parexel FSP challenges you to live up to your potential by joining us at SCRA, home-based, Spain.

We are looking for hard-working, talented, high-caliber people. We know that employee satisfaction leads to customer satisfaction, which is the ultimate driver of long-term success.

As the company that conducts vital clinical studies for sponsors, including the world's leading biotech’s and top 50 pharmaceutical companies, we offer you enormous security and long-term prospects.

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.

The most significant aspect of this position is that

- You will be dedicated to a single client

- You will be responsible for all site management and supervisory activities in the assigned oncology studies.

- You will work with industry leaders and subject matter experts.

- You will have the opportunity to mentor junior CRAs.

- You will work with world-class technology.

- You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.

From you we expect

- Extensive experience in site management, with knowledge of clinical trial methodology and terminology.

- Experience in oncology trials, at least 3 years.

- Minimum 3 years’ experience in independent supervision of all types of visits.

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

- Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines.

Our people and their passion are very important to us as they are the key to our success. That's why we provide you with an open and friendly working environment where we empower people and provide them with opportunities to develop their careers in the long term. In addition, you will have the opportunity to develop within your role and take on more responsibility or develop your skill set within other related Parexel FSP departments.

For an immediate interview, please contact marta.kuniewicz@parexel.com

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