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Clinical Scientist (1043904)

Remote: 
Full Remote
Contract: 
Salary: 
140 - 170K yearly
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Degree in Life Sciences preferred, 5+ years of clinical science experience, Proficient in GCP/ICH guidelines, Ability to write regulatory documents, Basic understanding of relevant disease area.

Key responsabilities:

  • Analyze and interpret clinical trial data
  • Lead preparation for study meetings
  • Collaborate with clinical development team
  • Contribute to writing regulatory documents
  • Implement clinical biomarker strategy
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Job description

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Your missions

Location: NEW YORK, NY, USA

Salary: $140,000.00 USD Annually - $170,000.00 USD Annually

Description: Our client is currently seeking a Clinical Scientist for a permanent/direct hire position that can sit remotely, but will require occasional onsite visits to the NYC area.

Description

  • Review, analyze, and interpret emerging clinical trial data (including biomarkers, clinical pharmacology, and safety data) and lead preparation for key study meetings (e.g. investigator meetings, monitoring committees, advisory boards)
  • Collaborate with the medical monitor on oversight of clinical trial activities, including safety reviews and site interactions.
  • Communicate with the broader clinical development team (clinical operations, data management, and regulatory teams)
  • Contribute to the writing of key study and regulatory documents (e.g. protocol, ICF, study manuals, briefing books)
  • Lead internal meetings to review topics and develop mitigation plans.
  • Contribute to the creation of presentations, abstracts, and publications emerging from clinical and translational studies.
  • Work with clinical and research teams to implement the clinical biomarker strategy for early phase clinical studies.
  • Ensure all activities comply with ICH/GCP guidelines, applicable regulatory requirements, and SOPs
  • Perform other duties as assigned.

Required Education/Qualifications/Skills:

  • A degree in Life Sciences (MD, PhD, Pharm D, MS or similar scientific field preferred).
  • At least 5+ years of experience in clinical science, clinical research, or equivalent is expected.
  • Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.
  • Basic understanding of disease area, compound, current clinical landscape.
  • Ability to write regulatory documents and lead clinical scientist tasks.
  • Knowledge and skills to support program-specific data review and trend identification.
  • Advanced medical writing skills and medical terminology.
  • Basic knowledge of the establishment and operation of data monitoring committees, medical review teams, and adjudication committees.

Contact: jgearhart@judge.com

This job and many more are available through The Judge Group. Find us on the web at www.judge.com

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Human Resources, Staffing & Recruiting
Spoken language(s):
Check out the description to know which languages are mandatory.

Soft Skills

  • Verbal Communication Skills
  • Problem Solving
  • Collaboration

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