MSD

H1B vizasi homiysi Biotexnologiya Logistika Sog‘liqni saqlash

MSD saraton, yuqumli kasalliklar, yurak-qon tomir va metabolik holatlar, shuningdek, profilaktik tibbiy yordam kabi muhim sog‘liq muammolariga qarshi dori vositalari va vaksinalarni ishlab chiqadigan global biofarmatsevtika kompaniyasidir. Amerika Qo‘shma Shtatlari, Kanada va Puerto-Rikoda Merck & Co., Inc. nomi bilan tanilgan MSD ilmiy tadqiqotlarni ishlab chiqish va tijoriy tajriba bilan birlashtirib, odamlar va hayvonlar uchun tibbiy yechimlarni taqdim etadi.

Kompaniya faoliyati Inson salomatligi, Hayvonlar salomatligi hamda Tadqiqot va ishlanmalar yo‘nalishlarini qamrab oladi. Bu ilmiy, klinik, tijoriy, operatsion va korporativ jamoalarda faoliyat yurituvchi mutaxassislar uchun imkoniyatlar yaratadi. Dunyoning turli hududlarida faoliyat olib boradigan MSDdagi martaba imkoniyatlari tadqiqot, hamkorlik, inklyuzivlik va global salomatlik sohasidagi mas’uliyatli taraqqiyotga e’tiborni aks ettiradi.

Kompaniyadagi ish o‘rinlari

Clinical Research Associate Manager, Neurology — MSD

Lead a team of clinical research associates overseeing neurology trial monitoring, site performance, and compliant study delivery at MSD. The role also covers team development, resource planning, and coordination with clinical and operational partners.

3 kun oldin

Amerika Qo‘shma Shtatlari

Nyu-Jersi

142 400 $ – 224 100 $ / yil

Masofaviy To‘liq stavka O‘rta daraja Talab Qilinadigan Til: inglizcha Klinik tadqiqot

Google Cloud Platform

Tavsif

Lead and support a team of 6–14 Clinical Research Associates.
Monitor study and site performance for compliance with local regulations, company procedures, and ICH GCP.
Train, mentor, support, and review CRA performance while guiding career development.
Address performance concerns and resolve escalated operational issues.
Assign work and promote effective use of team resources.
Support capacity planning, staffing reports, and CRA workload forecasts.
Coordinate processes and protocol implementation with CRAs, partner line managers, clinical research managers, and other functions.
Work with clinical sites to resolve operational challenges.
Attend local investigator meetings when requested.
Partner with the Global Clinical Trial Organization on trial execution.
Refer site performance concerns to the Clinical Research Manager and Clinical Research Director.
Coordinate with local human resources and finance teams.
Maintain CRA adherence to company policies, procedures, and quality standards.
Travel up to 50%.

Talablar

Bachelor’s degree in a scientific discipline.
At least five years of clinical research experience.
At least three years monitoring clinical trials as a CRA.
Line management experience preferred; team leadership experience is the minimum.
Fluency in the local language.
Business-level spoken and written English.
Strong knowledge of applicable ICH/GCP regulations and Good Documentation Practices.
Expertise with core clinical trial management systems and tools.
Ability to work independently and collaboratively.
Strong people, time, project management, and organizational skills.
Leadership, interpersonal, communication, and conflict resolution skills.
Ability to build relationships and communicate effectively with external customers, sites, and investigators.
Availability for travel up to 50%.
Must reside in the United States or Puerto Rico.
Visa sponsorship is unavailable.

Imtiyozlar

Annual bonus.
Long-term incentive, where applicable.
Medical, dental, and vision coverage.
Additional insurance coverage for employees and family.
Retirement benefits, including a 401(k).
Paid holidays.
Vacation leave.
Compassionate and sick leave.
Remote work arrangement.
Relocation assistance is not available.

O‘xshash ish o‘rinlari

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