صاحب العمل نشط
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكترونيحالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكترونيNot Mentionedسنوات
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أي جنسية
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1 وظيفة شاغرة
As a Clinical Trial Manager, you will lead and manage clinical trials from initiation through to completion, ensuring all project aspects are executed effectively. This involves overseeing timelines, budgets, and resources to ensure that trials are conducted efficiently and meet set objectives. You will play a critical role in ensuring compliance with Good Clinical Practice (GCP), regulatory requirements, and ethical standards, maintaining the integrity and quality of the trials.
Collaboration is key in this role. You will work closely with cross-functional teams, including clinical research associates, data managers, and biostatisticians, as well as external stakeholders such as sponsors and regulatory bodies. Your ability to foster effective communication and teamwork will be vital in navigating the complexities of clinical research and ensuring that all parties are aligned with the study goals.
Another essential responsibility is identifying potential risks that could impact trial progress. You will implement proactive solutions and contingency plans to mitigate these risks, ensuring that trials stay on track and within budget. This requires not only strong analytical skills but also the ability to adapt to changing circumstances and make informed decisions.
Requirements:
To qualify for this role, candidates should possess a minimum of two years of experience in clinical trial management. A strong understanding of GCP and regulatory guidelines is essential, as it ensures that all trials adhere to the highest standards of quality and compliance.
Excellent organizational skills are crucial, as you will be managing multiple projects simultaneously, each with its own unique challenges and timelines. You must be adept at prioritizing tasks and managing resources effectively to ensure that deadlines are met without compromising quality.
In addition to organizational skills, effective communication is paramount. You will be the primary point of contact for various stakeholders, requiring you to convey complex information clearly and concisely. Your ability to build strong relationships and facilitate collaboration among diverse teams will contribute significantly to the success of the trials.
Candidates should also demonstrate a proactive approach to problem-solving, with the ability to anticipate challenges and implement effective solutions. Your attention to detail and commitment to ethical standards will be instrumental in maintaining the integrity of the trials.
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