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A leading clinical research organization is seeking a Director of Clinical Development to manage client relationships and oversee strategic growth. This fully home-based position requires significant experience in clinical development and strong leadership skills. You will lead client meetings, manage the RFP process, and ensure compliance with quality standards. The ideal candidate has over 10 years of experience in a CRO and a strategic mindset. The role offers competitive compensation and opportunities for professional growth.
Director of Clinical Development, you will be responsible for overseeing client relationships, contributing to strategic business growth, and managing critical processes such as Requests for Proposals (RFPs). This role requires collaboration with cross-functional teams, including Clinical Operations and Business Development, to ensure the successful acquisition and management of clinical projects. You will be the main point of contact for clients from the initial engagement through contract closure.
This is a fully home-based role in one of the countries where OPIS has its affiliate - please check our website for more details on location.
We offer a competitive salary and benefits package as well as opportunity to be part of a company that values growth, innovation, and customer success. Please read the information notice on the processing of personal data in the candidates’ information section of our company website.
OPIS is an International CRO with over 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects. OPIS extensive expertise covers all phases of drug-related trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.
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