Lead Local Study Teams (LST) at the country level to deliver clinical studies according to agreed resources, budget, and timelines.
Ensure compliance with procedural documents, international guidelines and relevant local regulations.
Identify sites and perform site qualifications; set up, initiate, monitor, close sites and archive documentation.
May visit sites as needed to support the flexible capacity model.
Overall responsibility for study commitments within Turkey and timely delivery of data to required quality as per SMA.
Lead and manage LST(s) consisting of CRAs, start-up specialists, and study administrator(s); collaborate with sponsor and global Parexel teams.
Requirements
Bachelor’s degree in a related discipline, preferably in life science, or equivalent qualification.
Minimum 3 years of experience in Development Operations (CRA, SrCRA) or other related fields (Medical Affairs-led or Academic-led studies).
Experience of ICF preparation essential.
Experience of leading clinical trials.
At least 1 year project management experience.
Good knowledge of international guidelines ICHGCP as well as relevant local regulations.
Proven ability to lead and motivate cross-functional teams to deliver clinical trials according to or ahead of time plan, budget, and with required quality.
Excellent project management skills.
Ability to work home-based and attend sponsor office in Istanbul, Ankara, or Izmir (hybrid) as required.
Benefits
Home-based employment (permanent full-time)
Hybrid model: 3 days/week at sponsor office (Istanbul, Ankara, or Izmir)
ATS Keywords
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