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Clinical Trial Manager at KellyOCG

Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree in Life Sciences, 5-10 years of clinical research experience, Strong knowledge of ICH-GCP and regulations, Excellent decision-making and leadership skills, Proficient in English and relevant IT skills.

Key responsabilities:

  • Oversee full lifecycle of clinical trials
  • Act as primary contact managing timelines and recruitment
  • Prepare and manage trial budgets and contracts
  • Ensure timely reporting and compliance checks
  • Coordinate cross-functional teams for study conduct
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KellyOCG
1001 - 5000 Employees
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Job description

Note: This role is expected to potentially open in October. We are currently pipelining candidates for this position.

Location: Europe


Kelly FSP is searching for Clinical Trial Managers to support the global trials of our client, one of the top 5 pharmaceutical companies in the world. This remote role will involve working closely with the EMEA team.


With our FSP model, we welcome both freelancers and employees who want to join a global talent pool, work on exciting projects, and be exposed to cutting-edge technology.


Role Overview:

The Clinical Trial Manager will be responsible for end-to-end project management of global studies, including study start-up, vendor management, budgeting, and study close-out. Specific therapeutic areas and study phases will be assigned based on the candidate's interest and experience.


Main Responsibilities:

  • Oversee the full lifecycle of clinical trials, ensuring compliance with country-specific regulations, SOPs, and ICH-GCP guidelines.
  • Act as primary contact for assigned trials, managing timelines, patient recruitment, and study progress.
  • Prepare and manage trial budgets, including vendor contracts and cost reconciliation.
  • Ensure timely reporting and documentation of AEs/SAEs/PQCs and compliance with inspection readiness.
  • Coordinate cross-functional teams for data management and study conduct.
  • Maintain complete and accurate trial data and documents in CTMS and VTMF systems.


Qualifications:

  • Bachelor's degree in Life Sciences or equivalent.
  • Minimum 5-10 years of clinical research experience in the pharmaceutical industry or CRO.
  • Strong working knowledge of ICH-GCP, SOPs, and local regulations.
  • Excellent decision-making, leadership, and financial management skills.
  • Proficient in English (written and spoken).
  • Strong IT skills in relevant software and company systems.


Job Requirements:

  • Effective end-to-end project management experience.
  • Analytical mindset with a proactive approach to risk management.
  • Real-world evidence experience is a plus.
  • Experience in collaborative, outsourced, interventional, and non-interventional studies is preferred.



If you're interested in this role, apply now and join our global team at Kelly FSP. Alternatively, if you know someone who would be a great fit for this position, feel free to share the job posting with them.

Required profile

Experience

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

Other Skills

  • Leadership
  • Decision Making
  • Analytical Thinking
  • Technical Acumen
  • Verbal Communication Skills
  • Budgeting

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