Clinical Trial Manager
- Turkey
- ICON Strategic Solutions
- Clinical Trial Management
- Remote
Senior Talent Acquisition Business Partner
- Icon Strategic Solutions
About the role
As a Local Study Associate Director, you will be leading the Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with AZ Procedural Documents and international guidelines such as ICH-GCP as well as relevant local regulations.
In addition to leading LST(s), as the Local Study Associate Director (LSAD) you may perform site monitoring as needed to support the flexible capacity model.
• Has the overall responsibility for the study commitments within the country and for
timely delivery of data to required quality.
• Leads Local Study Team consisting of CRAs, CTAs, and Study Start-up Specialists for
assigned study/studies
• Leads and optimizes the performance of the Local Study Team(s) at country level
ensuring compliance with SOPs, ICH-GCP and local regulations.
• Ensures, as required, that clinical and operational feasibility assessment of potential
studies is performed to the highest quality.
• Coordinates the site selection process by identifying potential sites/investigators,
performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits
to evaluate suitability and quality risks.
• Ensures timely preparation of country financial Study Management Agreement (fSMA)
and maintains accurate study budget in the clinical studies financial system by regular
checks of the system and financial reports
• Bachelor’s degree in related discipline, preferably in life sciencqualification (*).
•Min 5 years experience in Clinical research , at least 1 year LSAD experience is preferable
• Good knowledge of international guidelines ICH-GCP as well regulations.
• Proven ability to lead and motivate cross-functional teams to deaccording to or ahead of time plan, budget and with required qu
• Excellent project management skills.
• Excellent team building and interpersonal skills.
• Excellent organizational skills.
• Excellent verbal and written communication skills.
• Excellent ability to prioritize and handle multiple tasks.
• Excellent attention to details.
• Excellent knowledge of spoken and written English.
• Good negotiation skills.
• Good ability to learn and to adapt to work with IT systems.
•Oncology experience is must
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
![A picture of Debora Oh](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/0.0.0/img/Oi_Ywfaw1E2c5AjadgdpUA/75/debora-oh-thumbnail.jpg)
Teaser label
Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
![women working on a laptop](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/0.0.0/img/n2h6XJiZukZoTQjbEPLPPQ/75/clinical+project+manager.jpg)
Teaser label
Career ProgressionContent type
BlogsPublish date
02/17/2023
Summary
Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high stan
![A picture of holographic images coming out of an iPad](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/0.0.0/img/9Ha3P8C8O0Oc2AjadgdpUA/75/remote+decetralised+trials+2.jpg)
Teaser label
Inside ICONContent type
BlogsPublish date
10/03/2022
Summary
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the in-pe
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