Clinical Research Job at Chemo, Spain | Life Sciences | Apply Now
If you are a mid-career life sciences professional or clinical trials manager looking to leverage your bioequivalence and pharmacokinetic (PK) testing experience within an international corporate framework, this 9-month professional assignment is an exceptional opportunity. Located at Chemo’s advanced industrial operations and R&D facility in Azuqueca de Henares (Castile-La Mancha, Spain), this position inserts you directly into the operational lifecycle of global generic drug pipelines. For detail-oriented clinical coordinators searching for a high-impact Clinical Research Job, this position offers hands-on mastery over Clinical Research Organization (CRO) coordination, pharmacokinetic/bioequivalence (PK/BE) protocol development, and health authority scientific advice preparation. It serves as an elite corporate launchpad for a prominent life sciences job and stands out as a premier choice for professionals looking to secure an advanced job in Spain within a highly collaborative Contract Development and Manufacturing Organization (CDMO) ecosystem.
- Job Position: Junior Clinical Development- Temporary
- Location: Azuqueca de Henares, Castile-La Mancha, Spain
About The Company
INSUD PHARMA is a premier global healthcare corporation operating across the entire pharmaceutical value chain, delivering specialized scientific research, industrial synthesis, manufacturing, and international marketing of high-yield active pharmaceutical ingredients (APIs) and finished dosage forms (FDFs). The group employs over 10,000 professionals in more than 50 countries, leveraging a robust network of 20 state-of-the-art production plants, 15 specialized R&D centers, and 35 commercial affiliates worldwide.
Clinical Research Job – Key Responsibilities
The Junior Clinical Development Specialist acts as a crucial operational bridge, managing external clinical vendors and cross-functional teams to ensure trial timelines remain aligned with corporate product release objectives.
Your primary protocol management, monitoring review, and vendor oversight duties include:
- CRO Oversight & Coordination: Participating in the selection, contract tracking, and day-to-day supervision of external Clinical Research Organizations (CROs) to guarantee clinical trials are completed on time and within budget.
- PK/BE Study Management: Planning, designing, and supervising phase I pharmacokinetic (PK) and bioequivalence (BE) trials, alongside supporting global multi-center phase II and III studies to advance this Clinical Research Job.
- Dossier & Protocol Reviews: Leading the thorough review of study-specific documentation before, during, and after trials, including clinical protocols, Informed Consent Forms (ICFs), monitoring logs, and comprehensive Clinical Study Reports (CSRs).
- Regulatory Authority Interaction: Supporting localized strategic interactions with Health Authorities, including drafting responses to Deficiency Letters and organizing materials for official Scientific Advice procedures for a top-tier life sciences job.
- Cross-Functional Strategy Alignment: Collaborating with internal experts across Pharmaceutical Development, Regulatory Affairs, Pharmacovigilance, Legal, and Project Management to optimize global pipeline strategies.
- Trial Logistics Administration: Coordinating internal operational execution procedures, such as tracking investigational medical product (IMP) shipments and handling quality excursions.
- Quality Management & SOP Upkeeps: Maintaining site compliance by writing, updating, and reviewing clinical Standard Operating Procedures (SOPs) to uphold strict internal GCP standards.
Qualifications & Profile Requirements For Clinical Research Job
This corporate position is meticulously tailored for autonomous, detail-driven life scientists who possess the technical confidence to navigate international trial standards.
- Required Academic Criteria:
- Educational Foundation: A mandatory University Degree in relevant Life Science discipline.
- Postgraduate Specialization (Preferred): A specialized Master’s degree in Clinical Trials Monitoring, Clinical Trials Project Management, or Pharmaceutical Industry Operations.
- Required Experience & Language Proficiencies:
- Experience Tier: 3 to 5 years of practical laboratory or clinical operations experience operating in similar development roles, with exposure to generic drug methodologies, bioanalytical datasets, or dissolution data required for a successful job in Spain.
- Linguistic Mastery: Full professional fluency in English is mandatory for international data interpretation; a communicative proficiency in Spanish is highly preferred.
- Regulatory Literacy: Strong working knowledge of global trial regulations and guidelines, including ICH, EMA, FDA, and international GCP criteria.
- Professional Competencies:
- Proactive problem-solving capabilities paired with highly developed analytical thinking.
- Excellent organizational skills, meticulous attention to detail, and the ability to manage competing project priorities under hard deadlines.
- Availability to travel occasionally for corporate business needs (estimated at less than 5% of the schedule).
In short, the Junior Clinical Development Specialist position at Chemo is a definitive route to transitioning your scientific background into a high-visibility, international corporate clinical asset. Securing this appointment allows you to move past generalized data entry and take comprehensive charge of the CRO relationships, bioequivalence protocols, and regulatory submission dossiers that validate affordable generic therapeutics for global distribution networks. If you reside in Spain, hold a pharmaceutical or medical degree, and possess the required 3+ years of clinical operations exposure, apply today to secure this premier Clinical Research Job, launch a highly rewarding life sciences job, and lock in this outstanding job in Spain.
