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MSD
MSD
Sponsor pentru viza H1BAsistență medicalăBiotehnologieLogistică

MSD este o companie biofarmaceutică globală care dezvoltă medicamente și vaccinuri pentru provocări majore din domeniul sănătății, inclusiv cancerul, bolile infecțioase, afecțiunile cardiovasculare și metabolice, precum și îngrijirea axată pe prevenție. Cunoscută sub numele Merck & Co., Inc. în Statele Unite, Canada și Puerto Rico, MSD îmbină cercetarea științifică cu expertiza în dezvoltare și comercializare pentru a oferi soluții de îngrijire a sănătății oamenilor și animalelor.

Activitatea sa acoperă domeniile Sănătății Umane, Sănătății Animalelor și Cercetării și Dezvoltării, creând oportunități pentru profesioniști din echipe științifice, clinice, comerciale, operaționale și corporative. Prin activitățile desfășurate în regiuni din întreaga lume, carierele la MSD reflectă accentul pus pe cercetare, colaborare, incluziune și progres responsabil în domeniul sănătății globale.

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Locurile de muncă ale companiei

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.

USStatele Unite ale AmericiiNJNew Jersey
142.400 $ – 224.100 $ / an
RemoteNormă întreagăNivel mediuLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • 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%.

Cerințe

  • 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.

Beneficii

  • 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.

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