ERGOMED yra pasaulinė sveikatos priežiūros paslaugų grupė, padedanti biotechnologijų ir farmacijos įmonėms viso vaistų kūrimo ciklo metu. Jos verslo sritys apima „Ergomed Clinical Research“, „PrimeVigilance“ ir „ADAMAS Consulting“, teikiančias klinikinių tyrimų organizavimo paslaugas, farmakologinio budrumo ir medicininės informacijos palaikymą bei GxP audito paslaugas. Įmonė dirba onkologijos, retųjų ligų ir kitų sudėtingų klinikinių tyrimų srityse, o jos veikla apima maždaug 100 šalių.
Senior Clinical Research Associate II, Spain and Portugal
Monitor Phase II and III clinical trials for ERGOMED, a specialist contract research organization focused on rare diseases and oncology. Conduct site visits across Spain and Portugal.
Aprašymas
- Conduct pre-study, initiation, interim, and close-out monitoring visits on site or remotely in Spain and Portugal.
- Ensure study facilities and site staff remain suitable throughout each trial.
- Identify investigators and assess their qualifications, resources, facilities, equipment, and staff.
- Provide training to investigational site staff as needed.
- Assist with regulatory and ethics committee submissions when applicable.
- Contribute to clinical research that brings safe and effective pharmaceutical treatments to patients.
Reikalavimai
- Hold a college or university degree in life sciences, or an equivalent combination of education, training, and experience.
- Have extensive on-site monitoring experience in Phase II or III trials.
- Ideally, bring experience with complex trials, such as oncology or rare disease studies.
- Be fully proficient in English, Spanish, and Portuguese.
- Be able to plan, manage multiple tasks, and work in a dynamic team environment.
- Have strong communication, collaboration, and problem-solving skills.
- Be able to travel.
Privalumai
- Remote work.
- Work-life balance.
- A collaborative, international team environment.
- Career development opportunities.
- Early ownership and trust.
- A passionate, collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.