Spain Job Openings
Parexel
Senior Clinical Research Associate - Spain - FSP
November 7, 2024
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
For an immediate interview, please contact marta.kuniewicz@parexel.com
#LI-REMOTE
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.
- Extensive experience in site management, with knowledge of clinical trial methodology and terminology.
- Experience in oncology clinical trials or willingness to supervise them.
- Minimum 3 years’ experience in independent supervision of all types of visits and in oncology.
- 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.
For an immediate interview, please contact marta.kuniewicz@parexel.com
#LI-REMOTE
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