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

2 days left

Location
Norway
Salary
Negotiable
Posted
26 Apr 2021
Closes
10 May 2021
Ref
260421RZ03
Contact
Robert Zevallos
Hours
Full Time
Contract Type
Contract
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

THE ROLE

  • 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.

LOCATION

Norway

RATE

Competitive hourly rate

DURATION

4-month contract

1.0 FTE

REQUIRED

  • 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.

ABOUT i-PHARM CONSULTING

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.

www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Robert Zevallos on +44 (0)203 189 0486, or email rzevallos@i-pharmconsulting.com. 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.

KEYWORDS

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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