Freelance CRA/SSU - Norway - 4 months - 1.0 FTE

2 days left

26 Apr 2021
10 May 2021
Robert Zevallos
Full Time
Contract Type
Experience Level
Experienced (non-manager)

i-Pharm Consulting is seeking on behalf of a Top Global CRO a Freelance SSU Specialist. The home-based contract is ideal for candidates located in Norway. This an initial 4-month contract, our client is seeking an experienced individual who can come on-board with minimal training


  • Act as the client's direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase.
  • Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs), and any amendments.
  • Carry out Start-Up activities from site identification through pre-initiation
  • Conduct, drive, and manage country-specific feasibility and/or site pre-qualification and qualification activities,
  • Accountable for managing and driving the strategy for the Pre SIV / start-up tasks of the study
  • Prepare and submit IRB/IEC and MoH/RA (if applicable) application(s), resolving conflicts, determining appropriate follow up until receipt of final approval.
  • Submit all pertinent documentation to the trial master file as per project plans/sponsor/company policy.




Competitive hourly rate


4-month contract

1.0 FTE


  • Bachelor's degree in a scientific discipline or equivalent
  • Minimum 4 years of CRA experience
  • Advanced level study set up, site initiation, or study start-up experience or equivalent clinical operations experience working in a clinical research environment
  • Good understanding of both clinical trials methodology and terminology.


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology, and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance, and Bioinformatics.


If you would like to discuss this vacancy further, please call Robert Zevallos on +44 (0)203 189 0486, or email If this role is not suitable, Robert is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


CRA / Contract / Freelance / Clinical Research Associate / CRO / Contract Research Organisation / Pharma / Pharmaceutical / Medical Devices / Biotech / Biotechnology / Respiratory / Asthma / Cystic Fibrosis / Oncology / Breast / Pancreatic / Lung / Renal / Solid Tumour / Skin / Lymphoma and Non Hodgkin / Cervical / Melanoma / Friedreich's Ataxia / Multiple Sclerosis / Epilepsy / Migraine / Sleep Disorders / Neuropathic Pain / Malignant Pain / Fibromyalgia / London/ Phase II / Phase III / Monitoring / London i-Pharm / Home Based / Country / SCRA / Senior CRA / CTMS / EDMS / GCP / SOP / Oncology

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