Clinical Research Associate Job at Novotech, Spain | Life Sciences | Earn EUR 35,000 | Apply Now
If you are an experienced clinical monitor looking to advance your career with a global industry leader, this full-time position at Novotech is an exceptional opportunity. Located at the regional operations office in Madrid, Spain, this mid-level role places you at the strategic center of European clinical development. For structured relationship managers searching for a high-impact Clinical Research Associate Job, this position offers total ownership over site selection, source document verification, and patient safety tracking. It serves as an elite milestone for an enduring Novotech career and stands out as a premier choice for professionals tracking an advanced Life Sciences Job in Southern Europe.
- Job Position: Clinical Research Associate II
- Location: Spain
About The Company
Novotech is a globally recognized, full-service clinical Contract Research Organization (CRO) that has been a pioneer in drug development and scientific advisory services since 1997. Operating 30+ offices across the Asia-Pacific region, the United States, and Europe, Novotech specializes in providing biotechnology and pharmaceutical clients with an accelerated path to market for life-changing therapeutics. The company is highly celebrated for its award-winning workplace culture, earning distinctions as an Employer of Choice, Great Place to Work, and Employer of Choice for Gender Equality (EOCGE). Through its employee-centered “NovoLife” flexible benefits framework, Novotech empowers its global workforce with the trust, autonomy, and flexibility required to drive professional satisfaction and maximum results for clients.
Clinical Research Associate Job – Key Responsibilities
As a Clinical Research Associate II (CRA II), you will serve as the primary site relationship manager and central liaison between clinical investigational sites, Novotech project leaders, and pharmaceutical sponsors.
Your core operational, monitoring, and compliance duties will include:
- Site Relationship Management: Building strong, collaborative professional partnerships with Principal Investigators (PIs), study coordinators, and pharmacists to ensure smooth, expedited trial operations for this Clinical Research Job.
- Comprehensive Trial Monitoring: Executing on-site and remote monitoring visits in strict accordance with ICH-GCP §5.18 guidelines and study-specific Clinical Monitoring Plans (CMP). This includes managing Site Selection, Site Initiation, Site Monitoring, and Site Close-Out milestones, alongside unblinded pharmacy visits.
- Participant Safety & Rights Audits: Protecting trial participant well-being by performing meticulous Informed Consent Form (ICF) audits, confirming patient eligibility, validating protocol compliance, evaluating investigational drug compliance, and reviewing Adverse Events (AEs/SAEs) for prompt sponsor reporting.
- Data Verification & Query Resolution: Verifying that reported clinical trial data are accurate, complete, and fully verifiable from raw source documents, driving prompt resolution of electronic Case Report Form (eCRF) data queries.
- Investigational Product (IP) Accountability: Ensuring all study drugs and biologics are appropriately stored, dispensed, tracked, and reconciled at the site pharmacy level.
- Regulatory & Recruitment Acceleration: Collaborating with internal In-house CRAs and Regulatory Start-Up Associates (RSAs) to prepare essential documents and ethics filings, while driving site-specific recruitment plans to hit enrollment targets for this Life Sciences Job.
Qualifications & Requirements For Clinical Research Associate Job
This intermediate monitoring position is tailored for high-performing professionals who demonstrate strong critical thinking, analytical mindset, and rapid decision-making habits.
- Educational Foundation: A Graduate degree in a clinical, or life sciences-related field. Relevant qualifications in allied healthcare professions (Nursing, Pharmacy) will also be fully considered.
- Industry Track Record: At least 2 to 3 years of direct Clinical Research Associate (CRA) monitoring experience within a Contract Research Organization (CRO) or pharmaceutical environment is required to advance your Novotech career.
- Technical Skills: Deep, practical working knowledge of ICH-GCP guidelines, local Spanish clinical trial directives (AEMPS), and global regulatory frameworks. High computer literacy and familiarity with CTMS/eCRF software are required.
- Core Competencies: Exceptional interpersonal and team skills, excellent time-management habits, sharp attention to detail, and a strategic mindset capable of troubleshooting site-level bottlenecks independently.
- Logistics: Regular full-time schedule based out of the Madrid office (Calle Orense, 34 Torre Norte). Requires regional travel to investigational sites as dictated by the Clinical Monitoring Plan.
Compensation & Corporate Benefits
Novotech recognizes that driving global scientific impact requires a supportive corporate ecosystem that prioritizes equity and individual balance:
- Annual Base Salary: EUR 35,000 baseline (Final compensation will be aligned with the candidate’s specific experience level, technical skills, and internal equity).
- NovoLife Framework: Access to a customized, flexible corporate benefits plan designed to optimize your professional and personal work-life balance.
- Flexible Working Models: Supportive options for flexible working arrangements to help manage monitoring travel schedules effectively.
- Leave & Family Support: Inclusive leave entitlements, including paid parental leave accessibility for both parents.
- Wellness & Development: Comprehensive corporate wellness programs paired with structured ongoing development, professional training, and mentorship paths.
- Candidate Commitment: As a proud Circle Back Initiative Employer, Novotech explicitly commits to responding directly to every applicant.
In short, the Clinical Research Associate II position at Novotech Spain is a definitive route to transitioning your baseline clinical monitoring experience into a high-visibility, autonomous trial management asset. Securing this role allows you to step away from repetitive data collection and take full clinical ownership over multi-center clinical trials on the cutting edge of biotechnology. If you possess a life sciences background, 2–3 years of verifiable field monitoring experience, and a passion for patient safety, apply today to secure this premier opportunity.
