Senior Clinical Research Associate - FREELANCE - 0.2 - 0.4 FTE (España)

Senior Clinical Research Associate - FREELANCE - 0.2 - 0.4 FTE (España)

03 ago
|
Propharma
|
España

03 ago

Propharma

España

Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado.
Senior Clinical Research Associate - FREELANCE - FTE

Join ProPharma as a Freelance Senior Clinical Research Associate (SCAR) working 0.2–0.4 FTE in Spain.

Responsibilities

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- Manage one existing site and set up/monitor three new sites for a study.

- Conduct all types of monitoring: site initiation, interim, close‑out, co‑monitoring visits both in person and remote.

- Write and complete monitoring reports within SOP and local regulatory parameters.

- Perform study start‑up activities: site identification, feasibility, collection of essential documents, Ethics Committee submissions, and other site setup activities.

- Support development of study‑specific monitoring documentation (trackers, guidelines, plans, templates, tools).

- Review source documents and case report forms for accuracy, completeness and integrity, and resolve data issues.

- Manage investigational supplies: preparation, dispatch, return, inventory, and reconciliation.

- Monitor site enrollment, termination updates, protocol deviations, serious adverse events, lab abnormalities, and other activities contributing to trial conduct.





- Oversee regulatory documentation for accuracy and completeness; address regulatory concerns.

- Communicate with sites, investigators, client personnel and cross‑functional teams regarding monitoring and site‑management needs.

- Participate in meetings and conference calls with internal teams, sponsor teams, and external partners.

- Other duties as assigned.

Required Qualifications

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- Excellent verbal, written, interpersonal and presentation skills.

- Proficient in Microsoft Office (Outlook, Word, Excel, PowerPoint).

- Experience with EDC, CTMS, IVRS, and eTMF.

- Knowledge of local regulations, ICH Guidelines, and GCP.

- Ability to prioritize tasks, plan proactively, and accomplish goals with minimal supervision.

- Capable of providing solutions when obstacles arise and training as needed.

- Strong organizational skills and attention to detail.

Education

Bachelor’s degree or equivalent combination of education and experience.

Experience

More than 5 years as a Clinical Research Associate.

Employment Type

Contract. xqbhyrx

Location

Spain.

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

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