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PSI CROPC

Operations Manager, Clinical Trials

PSI CRO is a global, full-service Contract Research Organization (CRO) founded in 1995, specializing in predictable patient enrollment and on-time delivery of clinical trials across various therapeutic areas. Headquartered in Switzerland, PSI operates in over 50 countries with a strong focus on quality and client satisfaction.

PSI CRO

Employee count: 1001-5000

Turkey only

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Key responsibilities:

  • Lead the team in driving network growth by effectively engaging new clinics and healthcare partners.
  • Provide leadership, regular feedback, and development opportunities for team members.
  • Supervise the conduct of clinical trials in accordance with ICH GCP, applicable regulations, and internal procedures.
  • Foster a culture of transparency, accountability, and high performance.
  • Drive process optimization and standardization across all operational levels.
  • Assess feasibility of research protocols and select the most suitable studies for clinical sites.
  • Oversee budget negotiations, research timelines, and operational deliverables across assigned regions.
  • Manage and support Lead Coordinators by monitoring performance and ensuring alignment with quality standards.
  • Promote the Milestone One brand, build and maintain strong relationships with medical institutions, sponsors and CROs.
  • Co-develop operational procedures, templates, and guidelines for medical and site teams.
  • Supervise and support audit and inspection readiness.
  • Proven experience in clinical research operations management, preferably within CRO or Site Management Organizations (SMOs).
  • Strong leadership background with experience in team management and multi-site operations.
  • Comprehensive understanding of ICH GCP and operational aspects of clinical trials.
  • Excellent problem-solving, planning, and organizational skills.
  • Outstanding interpersonal and communication abilities.
  • Strategic mindset with a passion for process improvement and innovation.
  • Fluent English (additional languages are an advantage).
  • A key leadership role in a rapidly growing, innovative Site Enabling Organization (SEO).
  • Dynamic, international environment driven by collaboration and purpose.
  • Opportunity to influence the development of large clinical research networks worldwide.
  • Competitive remuneration and flexible form of employment (employment contract or B2B).
  • Global working model built on flexibility, trust, and continuous growth.

Milestone One, a pioneering Site Enabling Organization (SEO), is seeking an experienced Manager Operations to lead and expand our global operational structures across clinical research sites. This key leadership position is ideal for a strategic and hands-on professional who combines operational excellence with strong people management skills.

The successful candidate will be responsible for ensuring process consistency, high-quality trial execution, and ongoing improvement of operational standards across regions. Experience gained in Site Management Organizations (SMOs), especially within international or global environments, will be considered a strong asset.

About the job

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Posted on

Job type

Full Time

Experience level

Manager

Location requirements

Hiring timezones

Turkey +/- 0 hours

About PSI CRO

Learn more about PSI CRO and their company culture.

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We are a leading full-service global Contract Research Organization (CRO) with a key strength in predictable patient enrollment across multiple therapeutic areas. Since our founding in 1995 by Dr. Robert Reekie and Dr. Roger A. Smith, we've been dedicated to revolutionizing how clinical trials are conducted, focusing on delivering high-quality, cost-effective solutions worldwide. Our mission is to be the best CRO in the world as measured by our employees, clients, investigative sites, and vendors. This commitment is reflected in our exceptionally high repeat and referral business rates and minimal staff turnover.

Our global reach allows us to conduct clinical trials across multiple continents and in over 50 countries. We are known in the industry for our 'on-time project delivery,' a reputation we've built by investing substantial effort and medical expertise into performing quality feasibility assessments that provide accurate predictors of study timelines. In fact, over 90% of our studies finish on time or ahead of schedule. We specialize in planning and executing global pivotal registration clinical trials, particularly in complex areas like oncology, hematology, infectious diseases, gastroenterology, multiple sclerosis, and rare indications. We embrace innovation and technology, leveraging cutting-edge methodologies and data-driven insights to optimize trial design, streamline operations, and enhance patient engagement. Our robust quality management systems and adherence to the highest industry standards, including ISO 9001:2015 and ISO 27001:2013 certifications, underscore our dedication to excellence. We are proud of our contributions to advancing healthcare by helping bring life-saving therapies and treatments to market. We actively engage in research collaborations and knowledge sharing to contribute to scientific advancement.

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PSI CRO

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