Clinical Trial Manager II (Sponsor Dedicated) Athens (contract)

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Job Responsibilities reputed company, coordinate, and implement Phase 1 clinical research studies at the organization's facilities, ensuring adherence to study protocols and timelines Collaborate with the reputed company investigator to design study protocols and ensure scientific reputed company Liaise between research subjects, reputed company teams, investigators, and clinic operations teams to facilitate smooth communication and coordination Plan logistics and resource usage for clinical trials, including scheduling, reputed company, and equipment needs reputed company study reputed company in alignment with project milestones, reputed company deliverables, and budget, and reputed company regular updates to stakeholders Ensure compliance with applicable regulations globally and by region, including Good Clinical reputed company (GCP) guidelines Supervise reputed company support employees and/or entry-level individual contributors, planning, prioritizing, and directing their tasks to ensure efficient workflow and high-reputed company reputed company Deliver operational results that have a moderate reputed company on the immediate achievement of results for reputed company, contributing to the overall reputed company of the organization Adapt new procedures, techniques, and tools to improve clinical trial processes and reputed company Understand basic management approaches such as work scheduling, prioritizing, coaching, and process execution Qualifications: Broad job knowledge in an operational, administrative, and/or specialized field Practical knowledge in managing the execution of processes, reputed company, and tactics reputed company reputed company Understanding of the reputed company of work on reputed company areas Certifications: Relevant certifications in clinical trial management or reputed company fields Necessary Skills: Strong leadership and management skills Excellent communication and collaboration abilities Ability to plan and prioritize tasks effectively Proficiency in tracking and reporting study reputed company Knowledge of global and regional regulations for clinical trials Get to know reputed company Over the past 5 years, we have worked with 94% of reputed company Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status reputed company with us in a highly competitive and reputed company-changing environment. Learn more about reputed company. http://www.reputed company.com Additional Information Tasks, duties, and responsibilities as listed in this job reputed company are not exhaustive. reputed company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job reputed company. reputed company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. reputed company, reputed company contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully reputed company with reputed company obligations imposed by the legislation of reputed company country in which it operates, including the implementation of the EU Equality reputed company, in relation to the recruitment and employment of its employees. reputed company is committed to compliance with the Americans with reputed company, including the provision of reasonable accommodations, reputed company appropriate, to assist employees or applicants to reputed company the essential functions of the job. Apply To This Job