Role Description Dans le cadre d'un contrat de projet de 3 ans, le Département recrute un Psychologue clinicien. Le psychologue exercera pour 50% de son activité sur MADEO, service expérimental en partenariat avec le CHRU de Brest, et pour 50% de son activité pour les mineurs accueillis en dispositif individuel. Le psychologue a pour principales missions : - Exercer au sein de l’établissement en collaboration avec le responsable de service qui a autorité décisionnelle en matière d’orientation éducative pour les mineurs accueillis ou accompagnés. - Assurer l’accompagnement clinique des personnes accueillies au sein de MADEO / PAAS ou accompagnées par ses services. - Observer et analyser la dynamique individuelle de la personne accueillie ou accompagnée ainsi que le fonctionnement interne à la famille d’accueil. - Participer à la compréhension des situations, contribuer à l’analyse de la problématique du sujet et à l’élaboration de modalités d’accompagnement et d’orientation. Qualifications - Master 2 en psychologie exigé Requirements - Connaissances approfondies en psychologie clinique, psychopathologie et en psychologie du développement. - Sensibilité à la clinique de la parentalité. - Capacité d’identification et d’analyse des phénomènes transférentiels et contre-transférentiels. - Médiatisation des relations familiales. - Techniques d’entretien, d’aide à la formulation et à la restitution d’information. - Connaissance du cadre institutionnel relatif à la protection de l’enfance. - Capacité à activer un réseau médico-social. - Capacité à rédiger des notes psychologiques en tenant compte des règles éthiques en vigueur dans la profession. Benefits - Qualités d’écoute, capacité d’observation, d’analyse et de synthèse. - Sens du collectif et intérêt pour le travail en équipe pluridisciplinaire. - Discrétion professionnelle. - Capacité à la prise de distance et à la maîtrise de soi. - Qualité d’adaptation et de souplesse dans l’intervention. - Organisation, méthode et autonomie. Elements de candidature Pour postuler à cette offre, l'envoi du CV et d'une lettre de motivation est obligatoire.

• This position requires a candidate with extensive experience helping evidence generation strategy and execution of clinical studies. • The Clinical Study Manager-4 (CSM IV) role will develop and execute strategies for clinical and outcomes research studies to help regulatory approvals and key strategic evidence initiatives. • This role will be accountable for working with key stakeholders to design and develop clinical protocols and execute clinical studies (pre-market or post-market studies), with minimal supervision. • The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study. • The CSM will drive the progress of the trial during site selection, site start-up and through enrollment and follow-up. • The CSM will also take a leadership role in external communication with investigators and study teams.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Clinical Programs Director, Data Intelligence leads the creation and deployment of intelligent, data‑driven solutions that connect Salesforce with external molecule data to automate workflows, improve visibility, and strengthen operational performance. This role plays a critical part in advancing the Molecule Tracking Growth Room initiatives by streamlining and accelerating the spec win to design in process. The role will directly influence Cytiva’s ability to secure specification positions and expand market share in high‑value drug development workflows. This role reports to the Director, Clinical Programs Platforms and Strategy and sits within the Clinical Programs organization, based in Marlborough, Massachusetts, supporting initiatives across a global footprint. What you will do: - Lead the CRM Analytics roadmap for Design In, ensuring alignment with Clinical Programs strategy and commercial growth objectives while integrating Salesforce with external molecule datasets to enhance automation and visibility. - Provide technical and strategic leadership on AI driven tools that support molecule tracking, lifecycle management, and advanced analytics to accelerate specification wins. - Serve as the primary liaison with external analytics and technology partners, driving collaboration and successful delivery of data‑driven solutions. - Oversee the full development lifecycle—including solution design, prototyping, implementation, testing, deployment, and ongoing optimization—to deliver scalable analytics capabilities. - Deliver monthly Policy Deployment reporting, translating performance insights into clear, actionable recommendations for leadership. Who you are: - Bachelors degree in a scientific, technical, or related field. Masters degree preferred. - Deep experience with Salesforce, CRM Analytics (Tableau CRM/Einstein), SQL, and modern Microsoft tools, including Copilot and emerging AI platforms. - Demonstrated ability to design and execute CRM and data strategies supporting complex analytics, reporting, and workflow automation at scale. - Exposure to AI/ML tools with the ability to translate technical outputs into practical business applications for molecule tracking and lifecycle insights. - Strong analytical, problem solving, communication, and stakeholder‑management skills, with the ability to operate both strategically and hands on to build, test, and optimize solutions. Travel Requirements: - 25% travel to EMEA, USCAN, and APAC It would be a plus if you also possess previous experience in: - Hands on experience with biotherapeutic drug development, molecule progression, or process development, with the ability to tie scientific workflows to commercial and operational decisions. - Familiarity with GlobalData, clinical program management systems, and external molecule databases, with the ability to synthesize these sources into actionable insights. - Proven success navigating complex, global, matrixed organizations and driving alignment across commercial, scientific, and technical stakeholders. - Experience leading cross functional digital or analytics initiatives, including collaboration with external data, analytics, or technology vendors to deliver scalable solutions. - Demonstrated track record using data insights to enhance workflow efficiency, operational performance, and commercial outcomes such as specification wins or pipeline visibility. Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide. The annual salary range for this role is $175,000-$195,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law. #LI-MH3 Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! What the Clinical Trial Associate does at Worldwide As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately. What you will do - Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.) - Maintain and quality audit to assure the most recent revisions of documents are on project portals - Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File - Maintain version and quality control of project documentation and submit to trial master file - Assist with the tracking and maintenance of project related information, including site medical question and answer log What you will bring to the role - Excellent written and verbal English as well as fluency of the language of the country of location - Ability to handle multiple tasks and exercise independent judgment - Strong attention to detail and focus on quality of work - Strong organizational and problem-solving skills - Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint Your experience - Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role - Skill sets and proven performance equivalent to the above We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn. Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.