Knowledgeable Clinical Research Coordinator adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
Main Study Coordinator:
- terapeutic area experience: neurology, urology, oncology, psychiatrist, diabetology, (coordinating of phase II, III, IV),
- preparing visit templates according to protocol,
- IMP management (register in IxRS, storage, temperature monitoring),
- entering all data to eCRF (iMedidata, Inform, Viedoc, DataLabs, IBM Clinical Development etc.),
- scheduling subject visits and procedures according to protocol,
- veryfying of medical records,
- dispensing medical devices (for example: e-diary) and study drugs,
- completing study documentation and maintaining the ISF,
- packaging and shipping lab specimen,
- presence on monitoring visits,
- participation in Investigator Meeting.
GCP certificate (The Global Healt Network) 15JAN2026
IATA certificate (Mayo Clinic Laboratories) 08MAR2026
GCP certificate (The Global Healt Network) 15JAN2026
IATA certificate (Mayo Clinic Laboratories) 08MAR2026