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Job Title: Clinical Research Associate I/II

Location: Bengaluru, Karnataka, India

Company: PSI CRO AG

Employment Type: Full-time, On-site

Industry: Pharmaceutical Manufacturing

Company Size: 1,001-5,000 employees

Application: Over 100 applicants

About Us:
PSI CRO AG is a dynamic, global company founded in 1995, bringing together over 2,700 dedicated and passionate individuals. We are committed to caring for our staff, clients, partners, and the quality of our work. Our mission is to be on the front line of medical science, changing lives and bringing new medicines to those in need.

Job Description:
As a Clinical Research Associate I/II at PSI CRO AG, you will be at the forefront of communication with project stakeholders, ensuring the successful execution of clinical research projects across various therapeutic indications. Your role will involve building and maintaining relationships with clinical sites and investigators, focusing on the rights, safety, and well-being of subjects, and ensuring data compliance.

Key Responsibilities:

  • Conduct and report all types of on-site monitoring visits.
  • Participate in study startup activities.
  • Perform CRF (Case Report Form) review, source document verification, and query resolution.
  • Manage site communication and serve as the primary point of contact for in-house support services and vendors.
  • Communicate study progress with internal project teams.
  • Engage in feasibility research.
  • Support the regulatory team in preparing documents for study submissions.

Qualifications:

  • College/University degree in Life Sciences like B.Pharm, M.Pharm, msc, bsc, Pharm.D or an equivalent combination of education, training, and experience.
  • At least 1-2 years of independent on-site monitoring experience in India.
  • Experience with all types of monitoring visits in Phase II and/or III clinical trials.
  • Full working proficiency in English.
  • Proficiency in MS Office applications.
  • Strong ability to plan, multitask, and work in a dynamic team environment.
  • Excellent communication, collaboration, and problem-solving skills.
  • Willingness and ability to travel.

Additional Information:

  • Career Advancement: Advance your career in clinical research with opportunities for personal and professional growth.
  • Supportive Environment: Work closely with dedicated cross-functional teams and receive comprehensive support and ownership of your projects.
  • Training & Development: Extensive training programs and a friendly, collegial team atmosphere.
  • Benefits: Competitive salary and benefits package.
  • Working Conditions: Excellent working conditions with a true focus on people.

Application Link

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