Are you ready to drive the future of clinical operations development from the comfort of your own home? Looking to be in the heart of a company where precision meets purpose?
Proclinical is seeking a dedicated and experienced leader to oversee clinical activities for specific therapeutic indications or across multiple indications for an asset. You will co-lead the Clinical Development Team alongside the Medical Development Lead, ensuring the successful execution of clinical development plans. This position requires strong leadership, strategic planning, and collaboration skills to drive clinical trial operations and deliver high-quality outcomes.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Give strategic input and accountability for clinical activities within assigned therapeutic indications or programs.
- Develop and execute Clinical Development Plans in collaboration with cross-functional teams, ensuring alignment with timelines, budgets, and quality standards.
- Co-lead Clinical Development Team meetings, focusing on strategic discussions and decision-making.
- Oversee clinical trial budgets, timelines, and resource requirements, ensuring alignment with financial planning.
- Identify risks, propose mitigations, and ensure timely adjustments to plans as needed.
- Collaborate with Clinical Trial Managers and teams to ensure the creation of high-quality trial documents and operational plans.
- Participate in country and site selection processes, ensuring informed decisions and effective communication with stakeholders.
- Support vendor and Clinical Research Organization selection and management processes.
- Act as the primary point of escalation for trial management and operational issues.
- Ensure compliance with ICH-GCP guidelines and other regulatory requirements.
- Drive continuous improvement by sharing lessons learned across trials and programs.
- Mentor and support the growth and development of assigned staff, if applicable.
Key Skills and Requirements:
- Bachelor's degree in a relevant field (e.g., Biology, Biomedical Sciences, Pharmacy) or equivalent experience; advanced degrees are a plus Experience in managing outsourced models, including CROs and vendors.
- Background in rare diseases or autoimmune clinical trials is a plus.
- Knowledge of ICH-GCP guidelines and regulatory requirements.
- Strong leadership and interpersonal skills with the ability to build effective relationships.
- Experience in global strategic drug development and clinical operations.
- Proven ability to manage complex projects, prioritize tasks, and resolve issues proactively.
- Excellent written and verbal communication skills in English.
- Strong organizational skills with the ability to maintain a holistic view while managing details.
If you are having difficulty in applying or if you have any questions, please contact Camille Sandres at c.sandres@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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