MSD
MSD

MSD एक वैश्विक बायोफार्मास्युटिकल कंपनी है, जो कैंसर, संक्रामक रोगों, हृदय एवं चयापचय संबंधी स्थितियों और रोकथाम-केंद्रित देखभाल जैसी प्रमुख स्वास्थ्य चुनौतियों के लिए दवाइयों और टीकों को आगे बढ़ा रही है। संयुक्त राज्य अमेरिका, कनाडा और प्यूर्टो रिको में Merck & Co., Inc. के नाम से जानी जाने वाली MSD वैज्ञानिक अनुसंधान को विकास और वाणिज्यिक विशेषज्ञता के साथ जोड़कर लोगों और पशुओं तक स्वास्थ्य सेवाओं से जुड़े समाधान पहुँचाती है।

इसका कार्य मानव स्वास्थ्य, पशु स्वास्थ्य तथा अनुसंधान एवं विकास के क्षेत्रों में फैला हुआ है, जिससे वैज्ञानिक, क्लिनिकल, वाणिज्यिक, परिचालन और कॉर्पोरेट टीमों में पेशेवरों के लिए अवसर बनते हैं। दुनिया भर के विभिन्न क्षेत्रों में अपनी गतिविधियों के साथ, MSD का करियर-केंद्रित कार्य अनुसंधान, सहयोग, समावेशन और वैश्विक स्वास्थ्य में जिम्मेदार प्रगति पर इसके ध्यान को दर्शाता है।

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.

विवरण

  • 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%.

आवश्यकताएँ

  • 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.

लाभ

  • 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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