FREELANCE Country Approval Specialist - Denmark - Home-Based

i-Pharm Consulting are seeking on behalf of a leading Global CRO a Freelance Country Approval Specialist to start immediately. Home based contract ideal for someone based in Denmark or Sweden who has extensive experience preparing local Danish EC/RA submissions.

THE ROLE:
Other duties include:

• Prepare, review and coordinate initial Ethics Committee and Regulatory Affairs in Denmark
• Keep updated on local laws and regulations in Denmark
• Act as key contact at country level for local submissions
• Liaise with local sites on EC/RA submissions status
• Maintain trial status
• Support the development of local ICFs
• Ensure all timelines and deliverables are met for assigned projects

LOCATION:
Home based - Denmark/ Sweden

RATE:
Competitive hourly rate

DURATION:
6 months - high likelihood of extension

0.7 - 1.0 FTE

REQUIRED:

• Life science degree
• Strong experience within CROs
• Strong experience prioritising high workloads
• Significant experience within Study Start Up
• 3+ years in independently preparing initial EC/RA submissions in Denmark
• Ability to work independently
• Danish speaker

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 / Clinical Operations Coordinator / CRO / Contract Research Organisation / 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 / SSU / Study Start Up Specialist / Country Approval Specialist / Clinical and Regulatory Affairs Specialist / EC / RA / Denmark / Sweden / Regulatory Affairs / Ethics Committee / Copenhagen / Aarhus / Odense / Aalborg / Esbjerg / Randers / Kolding / Horsens / Vejle / Roskilde / Stockholm / Gothenburg / Malmo / Uppsala / Vasteras / Orebro