Data Engineer (F / H / X)

Council of Europe Development Bank; Paris; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

An established industry player is seeking Senior Clinical Research Associates to lead oncology studies in a dynamic and supportive environment. This role offers the unique opportunity to work closely with top-tier biotechs and pharmaceutical companies, ensuring the success of critical clinical trials. With a focus on manageable sites and protocols, you will enjoy a work-life balance while tackling exciting challenges in drug development. This position not only promises job security but also encourages personal and professional growth, allowing you to develop your skills and advance your career within the organization. If you are passionate about clinical research and want to make a difference, this role is for you.

Qualifications

• Substantial experience in site management and oncology clinical trials.
• Effective time management and problem-solving skills required.

Responsabilités

• Manage all site management and monitoring activities for oncology studies.
• Mentor junior CRAs and work with industry leaders.

Connaissances

Site Management

Clinical Trial Methodology

Time Management

Organizational Skills

Interpersonal Skills

Problem-Solving Skills

Outils

Clinical Research Software

Description du poste

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

Parexel is currently seeking Senior Clinical Research Associates in France with oncology experience. These will be home-based positions and fully dedicated to a single sponsor; however, successful candidates must be willing to work at least once a week from the sponsor's office in Paris. Candidates will ideally be based in Paris (or surrounding regions).

Working as a Senior Clinical Research Associate at Parexel 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.

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.

1. Responsible for all site management and monitoring activities across assigned oncology studies.
2. Work with industry leaders and subject matter experts.
3. Opportunity to mentor junior CRAs.
4. Work with world-class technology.
5. A pivotal role in the drug development process.

Here are a few requirements specific to this advertised role.

1. Substantial Site Management experience, with an understanding of clinical trial methodology and terminology.
2. Experience in, or willingness to monitor oncology clinical trials.
3. Experience in independent monitoring, all types of visits.
4. Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.
5. 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.