Skorzystaj z wyszukiwarki
Myślałeś o innych ofertach pracy? Skorzystaj z wyszukiwarki. OK, zrozumiałem.

Czy chcesz otrzymywać podobne oferty pracy dla "Clinical Research Warsaw", na email?

Utwórz powiadomienie e-mail

Filtry wyszukiwaniaFiltruj wyniki

  • Miejsce pracy
    • (36)
    • (2)
    • (1)
    • (1)
  • Region
    • (37)
    • (24)
    • (2)
    • (1)
    • (1)
  • Branża / kategoria
    • (15)
    • (14)
    • (6)
    • (5)
    • (4)
    • Zobacz więcej »
    • (3)
    • (3)
    • (3)
    • (2)
    • (2)
    • (2)
    • (2)
    • (2)
    • (1)
    • (1)
    • (1)
    • (1)
    • (1)
  • Min. poziom wykształcenia
    • (65)
    • (65)
    • (65)
    • (65)
    • (65)
    • Zobacz więcej »
    • (65)
    • (37)
    • (37)
    • (37)
    • (37)
  • Wymiar etatu
    • (65)
  • Okres publikacji
    • (6)
    • (28)
    • (37)
    • (42)
    • (48)
    • Zobacz więcej »
    • (52)

65 ofert pracy dla: Clinical Research Warsaw

Sortuj według:
  • start of a study. Major Duties and Responsibilities: Expertise in Clinical Research Data Management (DM) to provide oversight and advice to the clinical study team(s) regarding the DM activities and deliverables Development and oversight of DM processes and standards and functional leadership ...

  • Clinical Research Data Manager Warszawa NR REF.: 1100386 Currently for our Client, on of the world's most exciting bio-pharmaceutical companies, we are looking for a Clinical Research Data Manager.If you have minimum 1 year ofData Management experience in the Biotech/Pharma/CRO industry ...

  • education and ensure the end-user awareness. - Coordinate clinical trainings and lectures with speakers, and ensure the presence of the medical technology for all major congresses and symposiums by developing strong relationships with clinical Bodies like Anaesthesia, ICU, Neonatology and ER ...

  • study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions. - Creation/distribution of regulatory binders & the wet-ink signed documents binder - Assist study staff and

  • 2+ years experience in monitoring of medical device trials. - Fluent un French and English, Dutch would be a plus - Strong organizational and time-management skills. - Working knowledge of EU Directives / local regulations / device development, and clinical monitoring procedures ...

  • on logistic processes for research and expert panel meetings. REQUIREMENTS - Bachelor or Masters degree in pharmaceutical sciences or related area's - 1 year of experience with the Trial master file, and administrative experience. - Experienced in Microsoft Office

  • globally located, managers, directors and leaders of clinical study sites are delivered with the specific data and information they require. Working in this positions you must be aware of the processes restrictions and regulations. This may have you working with different data bases. You will have to not

  • years of experience, and a minimum of 1 years as a Clinical study manager - Fluent in English, additional european languages are a plus - Good knowledge and understanding of ICH-GCP / ISO14155 and the applicable Medical Device regulations Are

  • clinical master file. - Ervaring met Microsoft Office programma's - Oog voor details en organisatie vaardigheden - Vloeiend in de Engelse taal, Nederlands is een pluspunt Are you interested and do want to apply for this role, please fill out

  • research and development practices, scientific and quality terminology, company quality assurance procedures and policies, and quality evaluation techniques as well as adult training development expertise. Are you interested and do want to apply

  • strategic thinking, project management - focus on cooperation with customer and work in a team Senior Analyst (survey team)Miejsce pracy / Location Warsaw

  • Clinical Trial Research Agreements. Besides this an Operations Manager will: - Track financial forecasting of the operational budget in conjunction with Clinical Research Director - Execute and oversee the clinical trial country submissions and approvals for assigned protocols - Oversee and coordinate

  • Pharmaceutical Statistician Warszawa NR REF.: 1097408 Currently for our client, pharmaceutical companyin Warsaw, we are looking for Pharmaceutical Statistician. What will you be doing? In this position you will be responsible for providing statistical expertise to support the design and

  • Analyst in Centralized Monitoring Team Warszawa NR REF.: 1099372 Currently we are looking for Analyst in Centralized Monitoring Teamto join pharmaceutical company with an office in Warsaw, What will you be doing? While working at this position you will be responsible for : providing

  • with a solid background in Clinical Development, Data Analysis and Clinical Systems. Additionally you will have proven knowledge of clinical and pharmaceutical drug development process, understanding of GCP and regulatory requirements. You will have very good written and verbal communication skills in English ...

  • set-up of the electronic Trial Master File including tracking of documents. Maintain and close the eTMF ensuring International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) compliance Initiate and maintain production of study documents, ensuring template and version

  • a global pharmaceutical leader with more than 31,000 professionals working together across 70 countries. We have an unwavering dedication to put people first and we live our values ofTakeda-ism?Integrity, Fairness, Honesty, and Perseverance. We are united by our 235-year legacy of research Accountabilities include: Medical/Scientific Affairs Use specific disease and product knowledge to develop Takeda ...

Czy chcesz otrzymywać podobne oferty pracy dla "Clinical Research Warsaw", na email?

Utwórz powiadomienie e-mail
do góry