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Senior Clinical Research Associate

1 hour, 54 minutes ago
Turkey
Senior
Operations Specialist
Operations
Apply Now
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
View All Jobs 132

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 startup and monitoring activities, including identifying investigators and supporting regulatory submissions.
  • Conduct pre-study and site initiation visits.
  • Manage appropriately sized clinical trials and support Project Managers on larger studies.
  • Train and mentor junior staff members.
  • Interact directly with clients and participate in project and trial updates.
  • Initiate payments and contribute to proposal activities, including development and client presentations.
  • Identify study risks and propose mitigation solutions.
  • Support work with a limited number of studies to maintain protocol expertise.

Requirements

  • University degree in life sciences, pharmacy, another health-related discipline, or equivalent scientific/healthcare experience; licensed healthcare professional also accepted.
  • 3.5+ years of CRA experience in a CRO or pharmaceutical/biotech environment, or equivalent relevant experience and demonstrated competencies.
  • Significant site management experience or equivalent clinical research experience.
  • Oncology monitoring experience.
  • Excellent communication and organizational skills.
  • Ability to work effectively as a team player.
  • 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.
  • Graduate or postgraduate degree preferred.
  • Experience monitoring in rare and complex therapeutic areas preferred.
  • Experience monitoring EDC trials and HER records preferred.
  • Experience in biopharma or a relevant therapeutic area preferred.
  • Start-up experience preferred.

Benefits

  • Fully home-based work arrangement.
  • Reasonable travel expectations compared with typical CRA roles.
  • Average assignment of only one to two studies, supporting deeper protocol expertise and better work-life balance.
  • Opportunity to work in a smaller CRO where your input can have visible impact.
  • Support from direct line management.
  • Opportunity to train and mentor junior colleagues.
  • Employee contributions are valued and encouraged.
  • Equal Opportunity Employer protections and reasonable accommodation support during the application process.

Interested in this position?

Apply directly on the company website

Apply Now

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