Clinical Scientific Expert

3 weeks ago

Dublin, Dublin City, Ireland SRG Full time

This range is provided by SRG. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

SRG are hiring on behalf of a multinational Pharma client for 2-3 positions in the area of Clinical Scientific Expert within the pharmaceutical industry.

6 month temp contract, with possibility of extension or conversion to a Permanent position

€20/hour PAYE- temp (Salary is fixed, non-negotiable)

Hybrid working- onsite 3 days per week minimum in Dublin HQ

Please note that you MUST have EU/EEA/UK citizenship or hold a current valid work visa for Ireland. No Sponsorship considered.

This is a great Opportunity for a PhD Graduate or Postgrad Research Analyst to join a leading Pharmaceutical Organisation, gain expertise and progress into a variety of Scientific positions within various Therapeutic Areas / Fields of Clinical Studies.

The Clinical Scientific Expert plays a vital role in providing clinical and scientific support across all phases of clinical studies, ensuring adherence to established processes and regulatory standards.

Your Role will be to:

  • Develop subject matter expertise in disease areas and clinical data review tools & processes through engagement in the work & collaboration with colleagues
  • Conduct thorough clinical study data reviews, analyse trends & provide insights for Interim Analysis & Post Lock activities focusing on subject safety, eligibility and data integrity
  • Contribute to the development of Data Review Plans, Data Quality Plans & data review strategy, ensuring consistent implementation of study protocol elements
  • Collaborate on Clinical Trials CRF - Case Report Form Development and assist in the implementation of data capture tools
  • Contribute to process improvements in data review, identifying & implementing innovative analysis processes & tools
  • Support the development of study-level documents and regulatory submissions, collaborating with relevant functions
  • Provide support for pharmacovigilance activities if required
  • Develop training materials and provide training to Clinical Trial teams
  • Assist & present at study level meetings

Knowledge Required:

  • Minimum Qualification of one of the following is essential:
  • PhD Advanced degree in Life Sciences / Healthcare, BioSciences, Bio Medical or Biological areas, MPharm, MBBS, Advanced Medical Masters Degree or Doctorate in Medicine, Surgery or Clinical Therapeutic areas
  • Fluency in English (oral and written)
  • Proven ability to work with high-quality data that will support strategic decision-making in medical / Health / Pharmaceutical areas
  • Research Projects in academia or industry in areas such as Medical Research, Medicine, Physiology, Clinical Research, Diseases & Therapy / Therapeutic Areas, Pharmacovigilance, Pharmacology or other related Scientific Research
Seniority level
  • Associate
Employment type
  • Temporary
Job function
  • Analyst, Research, and Science
Industries
  • Pharmaceutical Manufacturing and Medical Practices
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