P h3 Senior Clinical Research Associate - FREELANCE - 0.2 - 0.4 FTE /h3 p Join Pro Pharma as a Freelance Senior Clinical Research Associate (SCAR) working 0.2–0.4 FTE in Spain. /p h3 Responsibilities /h3 ul li Manage one existing site and set up/monitor three new sites for a study. /li li Conduct all types of monitoring: site initiation, interim, close‑out, co‑monitoring visits both in person and remote. /li li Write and complete monitoring reports within SOP and local regulatory parameters. /li li Perform study start‑up activities: site identification, feasibility, collection of essential documents, Ethics Committee submissions, and other site setup activities. /li li Support development of study‑specific monitoring documentation (trackers, guidelines, plans, templates, tools). /li li Review source documents and case report forms for accuracy, completeness and integrity, and resolve data issues. /li li Manage investigational supplies: preparation, dispatch, return, inventory, and reconciliation. /li li Monitor site enrollment, termination updates, protocol deviations, serious adverse events, lab abnormalities, and other activities contributing to trial conduct. /li li Oversee regulatory documentation for accuracy and completeness;





address regulatory concerns. /li li Communicate with sites, investigators, client personnel and cross‑functional teams regarding monitoring and site‑management needs. /li li Participate in meetings and conference calls with internal teams, sponsor teams, and external partners. /li li Other duties as assigned. /li /ul h3 Required Qualifications /h3 ul li Excellent verbal, written, interpersonal and presentation skills. /li li Proficient in Microsoft Office (Outlook, Word, Excel, Power Point). /li li Experience with EDC, CTMS, IVRS, and e TMF. /li li Knowledge of local regulations, ICH Guidelines, and GCP. /li li Ability to prioritize tasks, plan proactively, and accomplish goals with minimal supervision. /li li Capable of providing solutions when obstacles arise and training as needed. /li li Strong organizational skills and attention to detail. /li /ul h3 Education /h3 p Bachelor’s degree or equivalent combination of education and experience. /p h3 Experience /h3 p More than 5 years as a Clinical Research Associate. /p h3 Employment Type /h3 p Contract. /p h3 Location /h3 p Spain. /p /p #J-18808-Ljbffr

📌 Senior Clinical Research Associate - Freelance - 0.2 - 0.4 Fte (Madrid)
🏢 Propharma
📍 Madrid