Clinical Research Associate I/ Clinical Research Associate II

3 weeks, 2 days ago
Full-time
Junior
Operations
Precision For Medicine

Precision For Medicine

Precision for Medicine is a specialized scientific services company that helps pharmaceutical and life sciences clients innovate, develop, and commercialize next-generation medical products. With a diverse team of experts, they offer comprehensive serv...

Pharmaceuticals
1K-5K
Founded 2012
$225M raised

Description

  • Monitor and own the progress of clinical studies at investigative sites.
  • Ensure studies are conducted, recorded, and reported in accordance with protocol, SOPs, ICH-GCP, and applicable regulations and standards.
  • Coordinate study start-up and monitoring activities, including identifying investigators and preparing regulatory submissions.
  • Conduct pre-study and initiation visits.
  • Manage site-level study execution across an average of one to two studies.
  • Identify potential study risks and propose mitigation solutions.
  • Support investigator meetings, site visits, and project team updates.
  • Collaborate with direct line management and project teams to support study delivery.

Requirements

  • University degree in a life science, pharmacy, or other health-related discipline, or equivalent experience in a scientific or healthcare discipline; licensed health care professional also accepted.
  • At least 6 months of CRA experience in a CRO or pharmaceutical/biotech setting, or equivalent relevant experience and demonstrated competencies.
  • Site management experience or equivalent experience in clinical research.
  • Oncology monitoring experience.
  • Excellent communication and organizational skills.
  • Strong teamwork and client-focused approach.
  • Experience using computerized information systems, electronic spreadsheets, word processing, and email.
  • Ability to travel overnight, with up to 60% travel on average and international travel as needed.
  • Fluency in English and Turkish.
  • Start-up activities experience preferred.

Benefits

  • Fully home-based role.
  • Reasonable travel expectations compared with typical CRA roles.
  • Focus on one to two studies on average, supporting deeper protocol expertise.
  • Opportunity to work in a smaller CRO where your voice and ideas can have influence and impact.
  • Support from direct line management.
  • Work-life balance emphasis.

Interested in this position?

Apply directly on the company website

Apply Now

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