MSD yra pasaulinė biofarmacijos bendrovė, kurianti vaistus ir vakcinas svarbiausioms sveikatos problemoms spręsti, įskaitant vėžį, infekcines ligas, širdies ir kraujagyslių bei medžiagų apykaitos sutrikimus, taip pat daug dėmesio skirianti prevencinei priežiūrai. Jungtinėse Amerikos Valstijose, Kanadoje ir Puerto Rike MSD žinoma kaip „Merck & Co., Inc.“. MSD derina mokslinius tyrimus su kūrimo ir komercine kompetencija, kad sveikatos priežiūros sprendimai pasiektų žmones ir gyvūnus.
Bendrovės veikla apima žmonių sveikatą, gyvūnų sveikatą bei mokslinius tyrimus ir plėtrą, todėl galimybių atsiveria įvairių sričių specialistams – nuo mokslo, klinikinės ir komercinės veiklos iki operacijų bei įmonės funkcijų. Įvairiuose pasaulio regionuose veikianti MSD karjera atspindi jos dėmesį moksliniams tyrimams, bendradarbiavimui, įtraukčiai ir atsakingai pasaulinės sveikatos pažangai.
Associate Director, Clinical Study Management – Atherosclerosis and Metabolism
Lead planning and delivery of clinical trials in a senior study management role at MSD, a pharmaceutical drug-development company. Coordinate global teams, vendors, stakeholders, and study operations.
Aprašymas
- Shape trial strategy and lead operational planning and delivery for one or more clinical studies.
- Apply advanced leadership and technical expertise within global, cross-functional teams.
- Develop team members’ project management, communication, and collaboration skills through coaching.
- Oversee clinical trial feasibility, planning, execution, and conduct.
- Lead the Clinical Trial Team (CTT).
- Guide study planning, development, and delivery, including operational reviews, issue escalation and mitigation, senior management presentations, cross-functional meetings, and governance.
- Coordinate work among internal and external stakeholders, country teams, vendors, and committees.
- Work with partners, vendors, and the vendor management team.
- Review protocols and other clinical documents, providing clinical operations input.
- Contribute as a subject matter expert or serve on process improvement teams.
- Coach, mentor, and support the development of junior colleagues.
- May manage direct and indirect reports, including assigning resources and overseeing professional development and performance.
Reikalavimai
- Bachelor’s degree plus 9 or more years of pharmaceutical, clinical drug development, project management, or medical field experience; master’s degree plus 6 or more years; or PhD/PharmD plus 2 or more years.
- A degree in life sciences is preferred.
- Strong understanding of clinical research regulations, including GCP and ICH.
- Ability to manage competing priorities and delegate work effectively.
- Ability to create realistic short- and mid-range project plans.
- Strong analytical, problem-solving, prioritization, conflict-resolution, critical-thinking, communication, writing, and presentation skills.
- Demonstrated leadership across programs, processes, meetings, and matrix environments.
- Proficiency with Microsoft Office or similar tools, including Excel, PowerPoint, Word, and Outlook.
- Required skills include adaptability, analytical problem solving, clinical data management, clinical study management, collaboration, attention to detail, ethical standards, Good Clinical Practice (GCP), stakeholder alignment, and strategic thinking.
- Visa sponsorship is not available.
- Travel requirement: 10%.
- Regular employee status.
- First or day shift.
- A valid driver’s license is not required.
- Relocation is not provided.
Privalumai
- Annual bonus.
- Long-term incentive, where applicable.
- Medical, dental, and vision coverage.
- Other insurance benefits for employees and their families.
- Retirement benefits, including a 401(k).
- Paid holidays.
- Vacation.
- Compassionate leave.
- Sick leave.
- Hybrid work arrangement.