p h3Senior Clinical Research Associate - FREELANCE - 0.2 - 0.4 FTE /h3 pJoin ProPharma as a Freelance Senior Clinical Research Associate (SCAR) working 0.2–0.4 FTE in Spain. /p h3Responsibilities /h3 ul liManage one existing site and set up/monitor three new sites for a study. /li liConduct all types of monitoring: site initiation, interim, close‑out, co‑monitoring visits both in person and remote. /li liWrite and complete monitoring reports within SOP and local regulatory parameters. /li liPerform study start‑up activities: site identification, feasibility, collection of essential documents, Ethics Committee submissions, and other site setup activities. /li liSupport development of study‑specific monitoring documentation (trackers, guidelines, plans, templates, tools). /li liReview source documents and case report forms for accuracy, completeness and integrity, and resolve data issues. /li liManage investigational supplies: preparation, dispatch, return, inventory, and reconciliation. /li liMonitor site enrollment, termination updates, protocol deviations, serious adverse events, lab abnormalities, and other activities contributing to trial conduct.



/li liOversee regulatory documentation for accuracy and completeness; address regulatory concerns. /li liCommunicate with sites, investigators, client personnel and cross‑functional teams regarding monitoring and site‑management needs. /li liParticipate in meetings and conference calls with internal teams, sponsor teams, and external partners. /li liOther duties as assigned. /li /ul h3Required Qualifications /h3 ul liExcellent verbal, written, interpersonal and presentation skills. /li liProficient in Microsoft Office (Outlook, Word, Excel, PowerPoint). /li liExperience with EDC, CTMS, IVRS, and eTMF. /li liKnowledge of local regulations, ICH Guidelines, and GCP. /li liAbility to prioritize tasks, plan proactively, and accomplish goals with minimal supervision. /li liCapable of providing solutions when obstacles arise and training as needed. /li liStrong organizational skills and attention to detail. /li /ul h3Education /h3 pBachelor’s degree or equivalent combination of education and experience. /p h3Experience /h3 pMore than 5 years as a Clinical Research Associate. /p h3Employment Type /h3 pContract. /p h3Location /h3 pSpain. /p /p #J-18808-Ljbffr

📌 Senior Clinical Research Associate - FREELANCE - 0.2 - 0.4 FTE (España)
🏢 Propharma
📍 España