Roche

Diagnostics

ClinicalSiteManager

Motherwell, United Kingdom FULL TIME Remote Friendly
The Brief

“Clinical Site Manager at Roche. Skills: Clinical study management, Site management, Regulatory compliance. Design, plan, coordinate, and conduct clinical research studies. Initiate, monitor, and complete clinical research studies”

What You'll Achieve.

Diagnose earlier; Develop faster; Personalise treatment; Improve healthcare outcomes globally; Get competitive products to patients faster; Generate comprehensive clinical evidence; Demonstrate product safety; Demonstrate product effectiveness; Demonstrate scientific validity; Facilitate smooth product registration; Facilitate product adoption; Facilitate product reimbursement globally; Save lives; Improve patient quality of life; Achieve business goals; Ensure operational excellence

Industry & Context.

Diagnostics
Problems you'll solve

Analyze and solve

What They're Looking For.

Must Have

Bachelor's degree in Science Degree preferably in Health Sciences like Clinical Diagnostics or engineering (or equivalent combination of education and work experience), working experience in either the Medical Device or Diagnostics industry, working experience in clinical study of IVD/Medical Device/Drug, experience particularly in the cardiovascular/metabolic indication and Near Patient Care or Point of Care, Excellent understanding of ICH GCP guidelines in the execution of clinical trials, Ability to make sound decisions, Ability to analyze and solve, Ability to make independent choices, Ability to take responsibility, Flexibility and adaptability to perform in a fast-paced, matrixed environment

Nice to Have

Experience with studies in an emergency department setting is a plus

What You'll Do.

and conduct clinical research studies

and complete clinical research studies

Deliver data generation methodologies

Ensure studies are delivered

Act as primary contact for study site personnel

Coordinate training and certification

Provide technical assistance to sites

Perform site assessments and qualification visits

Support site selection and activation

Manage key study site documentation

Oversee CROs for site management activities

Collaborate with international investigators

Gather feedback and opinions from laboratories or customers

How You'll Work.

Team & Collaboration

Collaborate with internal teams; Collaborate with external partners; Collaborate with patients; Work in local and global study teams; Work in virtual teams; Foster strong, collaborative relationships with cross-functional team members; Collaborate with internal stakeholders; Collaborate with external partners

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