Clinical Director, Scientific Site Communication and ...

Clinical Director, Scientific Site Communication and EngagementPay CompetitiveLocation Billerica/MassachusettsEmployment type Full-TimeJob DescriptionReq#: 261481Work Your Magic with us!Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.Your Role:As the Clinical Director, you will s erve as the clinical research and development lead responsible for clinical trial(s), site engagement, study oversight and execution of clinical trial activities in assigned projects. You will manage a cross-functional clinical program/study team to define clinical trial activities that best support the overall program site engagement strategy. Together with the Clinical Lead, you oversee the planning and management of clinical trial conduct, including leading efforts related to study initiation, enrollment and data monitoring as well as providing input to study design and interpretation of results, identify potential key hurdles for study recruitment and guide the teams to find practical solutions to ensure optimal site engagement and adherence to the recruitment objectives and quality. This role requires close collaboration and communication with key stakeholders involved in study recruitment and liaise with key personal directly on site and during meetings and conventions.FINANCIAL DIMENSIONTogether with the clinical program team contributes to cost-effective approaches to execute clinical programsServe as Clinical Director:Key member of the relevant clinical and study teamsLead all aspects related to clinical and scientific study site engagement for clinical trials (e.g. lead efforts for site selection, study start up, developing and executing a study enrollment plan, review and advise on study related procedures interacting with site engagement and capabilities of study participation. Contribute to strategies to ensure data quality from study sites).Ability to work with Key Opinion Leaders, Scientific Advisors and other key clinical site personal in the relevant therapeutic area to ensure scientific engagement and optimal awareness of clinical trialsProvide input on the preparation of clinical development plans, study concept sheets, study protocols in collaboration with clinical and project team members for assigned indication(s)/products or with external partners for collaborative studiesManage, mentor and develop assigned staff, as appropriateSupport the review, analysis and interpretation of study dataSupport communication of study results as assignedStay up to date in the assigned therapeutic area and sub-area including oversight of significant new developmentsContribute to the progress of the organization by providing input into assigned business process improvement workstreams and tasksLocation: Billerica, MA preferred; remote considered with travelTravel:Who You Are:Minimum Qualifications:Medical Degree (MD, PharmD or other equivalent)Minimum of 5 years industry or clinical experienceMinimum 1 year of (associated medical director / medical director, respectively) experience in the pharmaceutical or biotechnology industry preferred including knowledge of regulatory requirements in clinical developmentExperience in design, set up, conduct and evaluation of clinical trialsExperience working in a cross-functional multi-site team environmentAble to communicate effectively in EnglishGood medical writing skillsPreferred Qualifications:Board certification or expertise in related TA preferred but not mandatoryAbility to work in an intense, fast paced, global work environmentPro-active, problem-solving, constructive attitudeStrong oral and written communication skills, including presentations (posters, paper, seminars) to internal and external partiesAbility to collaborate in a seamless fashion with project/program/functional teams both face to face and remotelyAbility to process complex medical-scientific topics and translate them into clinical development scenariosAble to maintain familiarity with rapid progress in the fieldWhat we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!Apply now and become a part of our diverse team!If you would like to know more about what diversity, equity, and inclusion means to us, please visit KGaA, Darmstadt, Germany, a leading science and technology company, operates across healthcare, life science and electronics.NoticeTalentify is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.Talentify provides reasonable accommodations to qualified applicants with disabilities, including disabled veterans. Request assistance at or 407-000-0000.Federal law requires every new hire to complete Form I-9 and present proof of identity and U.S. work eligibility.An Automated Employment Decision Tool (AEDT) will score your job-related skills and responses. Bias-audit & data-use details: . NYC applicants may request an alternative process or accommodation at or 407-000-0000. #J-18808-Ljbffr

Created: 2025-09-17