MSD je globalno biofarmacevtsko podjetje, ki razvija zdravila in cepiva za reševanje ključnih zdravstvenih izzivov, vključno z rakom, nalezljivimi boleznimi, srčno-žilnimi in presnovnimi stanji ter preventivno zdravstveno oskrbo. V Združenih državah Amerike, Kanadi in Portoriku je znano kot Merck & Co., Inc. MSD združuje znanstvene raziskave s strokovnim znanjem na področju razvoja in trženja, da bi zdravstvene rešitve približalo ljudem in živalim.
Njegovo delo zajema zdravje ljudi, zdravje živali ter raziskave in razvoj, kar ustvarja priložnosti za strokovnjake v znanstvenih, kliničnih, komercialnih, operativnih in korporativnih ekipah. MSD deluje v regijah po vsem svetu, njegove karierne priložnosti pa odražajo osredotočenost na raziskave, sodelovanje, vključevanje in odgovoren napredek na področju globalnega zdravja.
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.
Združene države Amerike
New Jersey
PensilvanijaOpis
- 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.
Zahteve
- 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.
Ugodnosti
- 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.