
Local Clinical Trials Coordinator
Há 2 dias
As a Clinical Trial Manager, you will be responsible for overseeing the operational aspects of clinical trials at the local level. This includes managing assigned protocols from start-up through to database lock and closeout activities.
Key responsibilities include ensuring that trial documents/records are compliant with company Standard Operating Procedures (SOPs), International Conference on Harmonization for Good Clinical Practice (ICH-GCP), and regulatory requirements.
You will also prepare high-level budget estimates in response to requests for services, followed by detailed budget proposals. Additionally, you will ensure overall contract management, including review and approval of external service provider contracts, change orders, and delivery of services as per contract.
Required Skills & Qualifications- Minimum of 2 years of local trial management experience in the pharmaceutical industry or Contract Research Organization (CRO)
- Previous experience as a Clinical Research Associate
- Strong working knowledge of ICH-GCP, company SOPs, local laws and regulations, assigned protocols, and associated protocol-specific procedures
- Strong IT skills in appropriate software and company systems
- Excellent decision-making and financial management skills
- Proficient in speaking and writing English
- Good written and oral communication skills
This is an exciting opportunity to join a leading global provider of clinical research services and commercial insights. As a Clinical Trial Manager, you will have the chance to work on innovative medical treatments and contribute to improving patient outcomes and population health worldwide.
OthersIQVIA offers a dynamic and supportive work environment, where you will have the opportunity to collaborate with experienced professionals and develop your skills and expertise.
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