Clinical Study Operations Manager - FSP

extra holidays - extra parental leave - fully flexible
Work set-up: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Degree in biological sciences, pharmacy, or a health-related discipline, or equivalent nursing qualification., Extensive experience in clinical trial management., Strong leadership, communication, and organizational skills., Ability to work independently and exercise judgment..

Key responsibilities:

  • Manage study activities from start-up to close at the country level.
  • Implement start-up and site activation plans regionally and nationally.
  • Oversee vendor management and ensure timely study delivery.
  • Coordinate communication with local teams, stakeholders, and CRO partners.

Parexel logo
Parexel XLarge http://www.parexel.com
10001 Employees
See all jobs

Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel are currently recruiting for an experienced Local/Country focused Study Operations Manager to join Clinical Operations team of our Sponsor, a top global pharmaceutical company.

In the role of Country Study Operations Manager, you will be responsible for study and country level activities from start up through conduct and study close.

This will be a fully remote position in Israel.

Key Accountabilities:

  • Responsible for study management aspects of assigned studies, including vendor and budget management. You’ll be an influential member of the wider team.
  • Regional/Country/Study level implementation of Start Up and Site Activation Plans.
  • Responsible for country/study level Recruitment Strategy.
  • Responsible to support the development of study level plans.
  • Communication with the local team and internal stakeholders and CRO partner as applicable and as listed above to ensure efficient and timely study delivery of the agreed plans.
  • Responsible for study and/or country vendor management and oversight including follow up and coordination of vendor deliverables.
  • The Country Study Operational Manager I will be able to work independently and exercise their own judgement.

Skills and Experience:

  • For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to us is working with heart.
  • Extensive experience in relevant clinical trial management
  • Excellent leadership, communication, and organizational skills and ability to multi-task under limited direction and on own initiative.
  • Prior and demonstrable experience working at a senior level within Study start up preferred.

Education:

  • Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience.

Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Organizational Skills
  • Communication
  • Leadership
  • Multitasking

Operations Manager Related jobs