Monitor klinických studií / SCRA pro TOP farmaceutickou společnost / Bratislava

• Conduct trials in accordance with protocols, SOP’, local regulations and ICH-GCP guidelines, including: feasibility, sites selections, obtaining necessary approvals and documentation, site initiations, monitoring and SDV, management of site recruitment performance, trial supplies management, data cleaning activities, close-out and archiving.
• Meet all local and company requirements with respect to safety reporting in trails. Regularly updates and ensures timely and good quality data in IMPACT and other systems, if required.
• Closely cooperate with Project Management, Data Management and HQ throughout the trial to ensure milestones achieved.
• Maintain current knowledge of therapeutic areas and if required perform tasks of Local Trial Manager (LTM).
• Prepare payment orders required by the study, as well necessary study documentation.
• Meet the key milestones in the trial and reaches the recruitment goals.
• Execute high quality data from Sites Staff.

Práce v přední originální farmaceutické společnosti v HPP
Zázemí kanceláře v Bratislavě
Služební automobil, MT, NT
Řadu zaměstnaneckých výhod
Vzdělávací a rozvojové programy
Dobré mzdové ohodnocení odpovídající zkušenostem i výkonu
Nástup ihned / dohodou

Nemocnice, ambulantná lekárska činnosť, ostatná zdravotná starostlivosť

Global pharmaceutical company offering worldwide opportunities to employees. World leader in the insulin market with a market share of more than 50% by volume. Slovak affiliate has ambition to improve quality of patients’ life and bring innovation into the markets. With a newly created team in sales force as well newly formed management team, the Slovak affiliate is well prepared for the new challenges.