Global Study Manager and Project Coordinator

hace 3 semanas


Barcelona, Barcelona, España Syneos Health, Inc. A tiempo completo

**About Syneos Health, Inc.**

Syneos Health is a leading global contract research organization (CRO) that provides clinical development services to the pharmaceutical, biotechnology, and medical device industries.

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.

We believe in creating a workplace culture where everyone feels valued and empowered to contribute their best work.

**Job Title:** Global Study Manager and Project Coordinator

**Location:** Home-based in Spain

**Estimated Salary:** €60,000 - €80,000 per year

**Job Description:

Job Summary:

This role is responsible for managing multiple clinical studies from start to finish, ensuring compliance with regulatory requirements and timelines.

The successful candidate will have experience in project management, study coordination, and quality assurance, with a strong understanding of Good Clinical Practice (GCP).

Key Responsibilities:

  1. Manage study planning, execution, and closure activities, including study initiation, monitoring, and site management.
  2. Collaborate with cross-functional teams, including investigators, sponsors, and vendors, to ensure smooth study conduct.
  3. Ensure timely completion of study deliverables, including reports, summaries, and other documentation.
  4. Conduct quality control checks on study data and documentation to ensure accuracy and integrity.
  5. Maintain up-to-date knowledge of GCP, ICH, and other regulatory requirements relevant to clinical trials.
  6. Participate in ongoing professional development to enhance skills and knowledge in project management, study coordination, and quality assurance.

Requirements:

  • Bachelor's degree in a life science or related field.
  • Minimum 3 years of experience in clinical research, preferably in a CRO or pharmaceutical company.
  • Proven track record of managing multiple studies and projects simultaneously.
  • Excellent communication, organizational, and time management skills.
  • Strong analytical and problem-solving skills, with attention to detail.

Benefits:

  • Competitive salary and bonus structure.
  • Ongoing professional development opportunities.
  • Flexible working arrangements, including home-based work options.
  • A collaborative and dynamic work environment.
  • Opportunities for career growth and advancement.


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