Job Description
Your Core Responsibilities- As part of your role, you'll manage the comprehensive administration of clinical trials and sites. This includes everything from document tracking and safety report management to database updates.
- You will have the opportunity to collaborate on the management of clinical and non-clinical supplies, working in conjunction with other team members across various roles.
- Prepare, distribute, and archive clinical documents, including the responsibility of eTMF reconciliation and ensuring quality control.
- You'll contribute to site evaluation/validation, startup, and submissions by providing and collecting necessary forms/lists in a timely manner.
- Exhibit your organizational skills by supporting local investigator meetings.
- As a process Subject Matter Expert (SME), you'll share best practices, recommend improvements, and provide training to your team members.
- One of the exciting aspects of this role is the opportunity to mentor junior Clinical Trial Coordinators (CTCs), fostering their professional growth in our company.
Qualifications:
- We're seeking candidates who are fluent in local languages and possess business proficiency in English, coupled with excellent communication skills.
- A good understanding of Global, Country/Regional Clinical Research Guidelines and Good Documentation Practices is necessary for this role.
- Proficiency in IT skills, including MS Office and clinical IT applications, with a strong focus on MS Excel.
- Knowledge of ICH-GCP appropriate to the role, accompanied by effective time management, organizational, and interpersonal skills.
- The ability to thrive in a multicultural environment, with a high sense of accountability and urgency, is vital.
- We value independent, proactive problem solvers with a positive, growth mindset.
- A minimum of 3-5 years in Clinical Research or relevant healthcare experience, with completed job training or a Bachelor’s Degree.
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.