Associate Clinical Team Lead
R
RhoClinical Research
Spain. Poland. United Kingdom. LatviaFull-TimeMiddle
Salary not disclosed
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Job Details
- Languages
- English
- Experience
- 3 years of clinical research experience within the CRO, pharmaceutical, or biotechnology industry and at least 2 years of on-site monitoring experience
- Required Skills
- Project ManagementGCP
Requirements
- Bachelor's Degree in a life science, nursing, pharmacy or related field.
- 3 years of clinical research experience within the CRO, pharmaceutical, or biotechnology industry.
- At least 2 years of on-site monitoring experience.
- Proven leadership capabilities in a CRO or pharmaceutical setting.
- Strong knowledge of GCP and regulatory requirements.
- Familiarity with clinical trial processes and documentation.
- Demonstrated ability to manage multiple priorities and deliver on deadlines.
- Experience using clinical trial management software and EDC systems.
- Excellent interpersonal and communication skills.
- Ability to submit CV in English.
Responsibilities
- Provide support to CTLs in the end-to-end clinical execution of projects or programs.
- Track and monitor recruitment, study metrics, monitoring, and documentation activities.
- Ensure site compliance with ICH-GCP guidelines and applicable regulations.
- Collaborate with cross-functional teams to facilitate study deliverables.
- Support the development and management of clinical operation timelines, resourcing, and budgets.
- Assist with CRA and IHCRA project training, onboarding, and material development.
- Support protocol deviation review and reconciliation activities.
- Assist with the review and development of study protocols and clinical monitoring plans.
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