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Feasibility Lead

Comac Medical
Bułgaria, Sofia
praca zdalna
rekrutacja online
153 dni temu

Join Our Team for an Inspiring Career Journey

Embark on a fulfilling career as a Feasibility Lead with COMAC MEDICAL, a distinguished full-service provider of CRO and SMO in the pharmaceutical industry. Since its establishment in 1997, COMAC MEDICAL has expanded its presence in Central & Eastern Europe, boasting a team of 320 dedicated professionals and securing its position as a leader in clinical research.
Feasibility Lead
Feasibility Studies Responsibilities:
  • Perform diverse feasibility studies upon request.
  • Develop a feasibility strategy based on study specifics and company experience.
  • Effectively manage ongoing feasibility studies, addressing issues and timelines.
  • Directly communicate with potential sites, investigators, and referral specialists as needed.
  • Actively seek new potential sites and investigators.
  • Establish, oversee, and maintain the feasibility database.
  • Perform or support the final assessment of feasibility data.
  • Create feasibility questionnaires and other tools applicable for feasibility studies.
  • Follow up on requests related to the feasibility study process.
  • Provide relevant feasibility data upon project award.
  • Compile information gathered from different sources.
  • Assist the Quality group in reviewing and revising feasibility SOPs, working practices, and policies as needed.
Business Development Duties/Responsibilities:
  • Participate in marketing activities, client presentations, and proposal development.
  • Attend professional and industry meetings as a representative of Comac Medical.
General Responsibilities:
  • Professionally represent Comac Medical.
  • Stay informed about company policies to effectively represent the company perspective to the staff.
  • Strictly adhere to applicable position company policies and procedures.
Qualifications for the Role:
  • Graduate or postgraduate degree.
  • 3+ years in clinical research.
  • Thorough knowledge of the clinical research process, including all functional areas of clinical trial management.
  • Strong understanding of patient recruitment strategies and site selection considerations.
  • Working knowledge of current ICH/GCP guidelines and applicable country-specific regulations.
  • Excellent organizational, communication (verbal and written), and interpersonal skills.
  • Exceptional analytical skills.
  • Positive attitude and ability to interact with all levels of staff.
  • Proficiency in English.
  • Ability to work in a dynamic environment and meet tight deadlines.
  • Working knowledge of Word, Excel, and PowerPoint.
  • Join a team of knowledgeable, high-achieving, and experienced professionals.
  • Experience an international and diverse work atmosphere.
  • Take on challenging projects in various therapeutic areas, including early phases.
  • Enhance your professional skills and progress in your career development.
  • Enjoy competitive remuneration and access to professional training.