Clinical Research Associate Job at Thermofisher, Spain | Life Sciences | Clinical Research Opportunity | Apply Now
If you are an experienced clinical monitor ready to take the next step in global clinical trials, this Clinical Research Associate Job based in Madrid, Spain, is an exceptional opportunity. Working within PPD’s clinical research portfolio—a part of Thermo Fisher Scientific—you will be at the forefront of bringing life-saving cures to the market. Building a Thermofisher career means joining a high-caliber team that has supported the top 50 pharmaceutical companies and over 750 biotechs across 2,700 clinical trials globally over the last five years. For those seeking top-tier CRA Jobs with a blend of hybrid flexibility and significant field impact, here is a strategic breakdown of the CRA II role.
- Job Position: Clinical Research Associate II
- Location: Madrid, Spain
- Job ID: R-01352555
- Category:Â Clinical Research
About the Company
PPD is a leading global contract research organization (CRO) providing comprehensive, integrated drug development, laboratory, and lifecycle management services. As part of Thermo Fisher Scientific, the team is united by a singular mission: to enable customers to make the world healthier, cleaner, and safer. In this environment, your scientific expertise directly translates into actionable data that accelerates the delivery of treatments for the world’s most challenging health concerns.
Clinical Research Associate Job – Key Responsibilities
As a Clinical Research Associate II, you are the critical link between the sponsor, the CRO, and the investigational sites. You will manage clinical monitoring processes from site initiation to close-out, ensuring absolute compliance with ICH-GCP guidelines and protocols.
- Risk-Based Monitoring (RBM): Apply critical thinking and Root Cause Analysis (RCA) to identify site process failures. You will implement Corrective and Preventive Actions (CAPA) to bring sites into compliance and mitigate trial risks.
- Data Verification: Ensure uncompromising data accuracy through Source Document Review (SDR), Source Document Verification (SDV), and Case Report Form (CRF) reviews during both on-site and remote monitoring visits.
- Investigational Product (IP) Management: Assess IP accountability through physical inventory and strict records review.
- Site Lifecycle Management: Identify potential investigators, conduct site initiation visits, monitor ongoing compliance, and perform comprehensive trial close-out and material retrieval.
- Documentation & Reporting: Maintain audit readiness by ensuring all essential documents are complete. Provide real-time status tracking updates to the Clinical Team Manager (CTM) and update Clinical Trial Management Systems (CTMS).
Qualifications & Mindset Required For Clinical Research Associate Job
To succeed in this Clinical Research Associate Job, you need a solid foundation in life sciences combined with proven on-the-ground monitoring experience.
- Educational Foundation: A Bachelor’s degree in a life sciences-related field or an equivalent relevant formal academic qualification.
- Required Experience: At least 1 year of direct experience as a clinical research monitor (or successful completion of the PPD Drug Development Fellowship).
- Regulatory Expertise: A demonstrated, working knowledge of ICH-GCP, applicable global/local regulations, and procedural documents.
- Analytical Skills: Well-developed critical thinking abilities for deep investigation, root cause analysis, and problem-solving.
- Communication: Exceptional oral and written English and Spanish skills to effectively collaborate with medical personnel, sponsors, and internal project teams.
In summary, this Level II Clinical Research Associate Job is a defining milestone for clinical professionals looking to expand their global footprint. By securing this role in Madrid, you are not just managing site paperwork; you are actively safeguarding patient well-being and data reliability for the world’s leading pharmaceutical innovations. If you have the required monitoring experience and a readiness to travel, this is an unmatched opportunity to advance your Thermofisher career and stand out in the competitive landscape of international CRA Jobs.
