Start up Specialist Spain

Resourcing Life Science Ltd.

Spain

On-site

EUR 42,000 - 62,000

Full time

14 days+

Get a reply from this recruiter

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Resourcing Life Science Ltd. is assisting a Global CRO in Spain seeking a Start up Specialist to manage EC/CA submissions and ensure GCP compliance. You will coordinate translations, support phase II-III studies, and work closely with sponsors.

Fluent English and Spanish, strong communication, and at least one year in EC/CA submissions are required; this is a full-time on-site position in Spain.

Qualifications

  • Bachelor degree in life-science.
  • At least 1 year in EC & CA submissions within a CRO, Pharma or Biotech in Spain.
  • Experience in clinical studies phase II-III.
  • Fluent in English and Spanish.
  • Excellent communication skills.

Responsibilities

  • Responsible for CA & Ethics Committee (EC) submission.
  • Keep up to date knowledge of GCP and ICH Guidelines for clinical research.
  • Translation and coordination of translations for documents required for submissions.
  • Supervising study conduct according to GCP requirements and all applicable laws.

Skills

Fluent English
Fluent Spanish
Excellent communication skills

Education

Bachelor degree in life-science

Job description

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Start up Specialist office based in Spain.

Job Overview
  • Responsible for CA & Ethics Committee (EC) submission
  • Keep up to date knowledge of GCP and ICH Guidelines for clinical research.
  • Translation and co-ordination of translations for documents required for submissions.
  • Supervising study conduct according to GCP requirements and all applicable laws.
Key Requirements
  • Bachelor degree in life-science
  • Min 1 year in EC & CA submissions within a CRO, Pharma, Biotech in Spain
  • Experience in clinical studies phase II-III
  • Fluent English & Spanish
  • Excellent communication skills
  • FTE: 1.0

Tagged as: start up jobs

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Spain Start-Up Submissions Specialist
Spain Start-Up Submissions Specialist

Resourcing Life Science Ltd. • Spain

On-site
EUR 42,000 - 62,000
Regulatory and Start Up Specialist
Regulatory and Start Up Specialist

Precision Medicine Group • Madrid

On-site
EUR 60,000 - 90,000
Spain-based Regulatory & Start-Up Specialist for Clinical Trials
Spain-based Regulatory & Start-Up Specialist for Clinical Trials

Precision Medicine Group • Madrid

On-site
EUR 45,000 - 75,000
Regulatory & Start-Up Specialist — Spain
Regulatory & Start-Up Specialist — Spain

Precision for Medicine • Madrid

On-site
EUR 40,000 - 70,000
Regulatory & Start-Up Specialist, Spain – Portuguese Fluent
Regulatory & Start-Up Specialist, Spain – Portuguese Fluent

Precision For Medicine • Madrid

On-site
EUR 45,000 - 65,000
Spain Regulatory Start-Up Expert - Contracts & Budgets
Spain Regulatory Start-Up Expert - Contracts & Budgets

Precision Medicine Group • Madrid

On-site
EUR 60,000 - 90,000
Study Start-up Specialist
Study Start-up Specialist

BeOne Medicines Ltd. • Spain

On-site
EUR 46,000 - 58,000
Regulatory and Start Up Specialist at Precision for Medicine
Regulatory and Start Up Specialist at Precision for Medicine

Precision for Medicine • Madrid

On-site
EUR 40,000 - 70,000
Regulatory and Start Up Specialist (Portuguese speaker) at Precision for Medicine
Regulatory and Start Up Specialist (Portuguese speaker) at Precision for Medicine

Precision for Medicine • Madrid

On-site
EUR 50,000 - 70,000
Regulatory & Start‑Up Specialist — Spain
Regulatory & Start‑Up Specialist — Spain

Precision Medicine Group • Madrid

On-site
EUR 60,000 - 90,000