Clinical Research Coordinator
hace 1 semana
We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team at Innovaderm Research. As a key member of our site activation team, you will play a critical role in ensuring the successful execution of clinical trials.
Key Responsibilities- Prepare Investigator Sites for clinical trials by reviewing and approving essential documents.
- Establish site activation timelines and coordinate activities to meet planned timelines.
- Communicate with clinical sites during site start-up and ensure alignment of activities with study timelines.
- Collaborate with other functional departments to ensure site activation targets are met.
- Escalate risks to site activation schedules to the Project Manager.
- Collect, review, and file essential site documents.
- Ensure documentation is complete and of good quality for site activation.
- Manage the electronic Trial Master File (eTMF) and ensure regulatory documents are up-to-date.
- Collect and distribute documents from/to sites.
- Produce meeting minutes from project meetings.
- Maintain ADI logs and assign documents for internal project-specific training.
- Assist with drafting study documents and study plans.
- Act as the main point of contact for site correspondences.
- Assist with local ethics submissions and provide support to internal and external teams.
Innovaderm Research is a contract research organization (CRO) specializing in dermatology. We offer a stimulating work environment, attractive advancement opportunities, and a company benefits package. Our values are collaboration, innovation, reliability, and responsiveness.
We are committed to providing equitable treatment and equal opportunity to all individuals. As such, we will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.
We only accept applicants who can legally work in Spain.
Requirements- Bachelor's degree in a field relevant to clinical research or equivalent experience.
- Specialized graduate diploma in drug development is an asset.
- Experience in clinical research and the biotechnology, pharmaceutical, and/or CRO industry is an asset.
- Excellent oral and written skills in English.
- Excellent knowledge and competency in Word, Excel, and PowerPoint.
- Ability to prioritize assignments and work under pressure.
- Attention to detail and meet timelines.
- Quick learner, good adaptability, and versatile.
- Strong organizational, communication, problem-solving, and multi-tasking skills.
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