Indirizzo
Forma di lavoroParma, Italy Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds....
ClinChoice is searching for a Clinical Trial Assistant (CTA) to join an international pharmaceutical company, with a focus on Respiratory, Paediatrics, Rare Disease and Special Care. This is an office based, full-time opportunity for four months initially, in the Emilia-Romagna region of Italy.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts. Main Job Tasks and Responsibilities:
- Perform research on paper Trial Master Files to provide necessary information to fill in a storyboard of each requested Clinical Trial.
- Search paper documents to retrieve the information requested.
- Scan and keep record of the documents used for retrieving the information.
- Complete a template for Clinical Supply and another for Pharmacovigilance for each study.
- Bachelor's degree.
- Experience in clinical research or the healthcare-related industry, including as a Clinical Trial Assistant.
- Working knowledge of international regulatory and ICH-GCP guidelines.
- Experience with Trial Master Files (TMFs).
- Experience working as part of a large team with proven ability to make an active contribution to the team's performance and teamwork.
- Good documentation practices.
- Self-motivated and displays initiative.
- Able to communicate clearly and accurately in both written and spoken English and Italian.
- Effectively collaborates with team members.
- Proven organizational skills demonstrated by the ability to understand and prioritize instructions and deliver against commitments on time.
- Proficient skills across multiple computer applications including Microsoft Office, Impact, etc.
- Attention to detail.
- Excellent work-life balance
- Dedicated Line Manager
- Full performance and development process with end of year reviews
- Career opportunities within in ClinChoice, locally and globally
- Employee satisfaction survey - your feedback is important for continuous improvement
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key words: Clinical Trial Assistant, Assistant, CTA, Project Assistant, English, Clinical Trials, CRO, Clinical Research Organization, Clinical Research, IRB, Regulatory Documentation, TMF, EDC, Outsourcing, Contract, Temporary #LI-ONSITE #ENTRY #TEMPORARY #LI-EM1
