3 Clinical Tracking Jobs

As a Clin Ops Specialist/CTA based in Athens, your role at Syneos Health will involve performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. You will assist Clinical Monitoring staff with site management activities, serving as a Sponsor representative for assigned studies and ensuring compliance with protocol requirements and relevant guidelines by communicating with sites. Additionally, you will create and assist with maintenance of Trial Master File (TMF) and project files, participate in file audits, prepare site manuals and other documents, update clinical tracking information databases, and track incoming and outgoing clinical and regulatory documents. Your responsibilities will also include managing a shared mailbox, processing site requests, coordinating the ordering, packaging, shipping, and tracking of site supplies and materials, assisting with team meetings, preparing accurate meeting minutes and action items, handling receipt, tracking, and disposition of Case Report Forms and Queries, and maintaining awareness in the field of clinical research through necessary training. To excel in this role, you should possess a High School diploma or equivalent, good communication and interpersonal skills, and the ability to embrace new technologies. Some travel, up to 25%, may be required as part of the role. Syneos Health is dedicated to developing its employees through career progression, supportive line management, technical and therapeutic area training, peer recognition, and a comprehensive total rewards program. The company is committed to fostering a Total Self culture where authenticity is valued, and diversity of thoughts, backgrounds, cultures, and perspectives are embraced to create an inclusive work environment. If you are passionate about making a difference in the field of clinical research, and eager to work in a dynamic and innovative environment where your contributions matter, Syneos Health offers a rewarding opportunity to be part of a global organization that is driven to accelerate the delivery of therapies and change lives. Discover more about Syneos Health and the impactful work we do by visiting http://www.syneoshealth.com. Please note that the tasks, duties, and responsibilities outlined in this job description are not exhaustive, and the company reserves the right to assign additional responsibilities at its discretion. Qualifications may vary based on equivalent experience, skills, and education. Moreover, this description does not create an employment contract, and the company is committed to compliance with relevant legislation to ensure equal opportunities for all employees. Additionally, reasonable accommodations will be provided as per the Americans with Disabilities Act to assist employees or applicants in performing essential job functions.,

As a Clinical Ops Specialist at Syneos Health in Beijing/Shanghai, you will play a crucial role in ensuring activities are carried out in alignment with Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. Your responsibilities will include supporting Clinical Monitoring staff in site management activities, acting as a Sponsor representative for assigned studies, and maintaining communication with sites to ensure adherence to protocol requirements and study procedures. You will be responsible for creating and managing Trial Master Files (TMF) and project files, participating in file audits, preparing site manuals and reference tools, and updating clinical tracking information in databases. Additionally, you will track clinical and regulatory documents, manage a shared mailbox, process site requests, and coordinate the ordering, packaging, shipping, and tracking of site supplies and materials. Your role will involve assisting in team meetings, preparing accurate meeting minutes and action items, and handling the receipt, tracking, and disposition of Case Report Forms and Queries. By completing all necessary training, you will maintain awareness of developments in the field of clinical research. To qualify for this position, you should have a High School diploma or equivalent, possess strong communication and interpersonal skills, and be adaptable to new technologies. The role may require minimal travel of up to 25%. Syneos Health is dedicated to fostering a supportive and inclusive work environment where employees are encouraged to be their authentic selves. We believe in continuous development and progression, offering career growth opportunities, technical training, peer recognition, and a total rewards program. We are committed to building a diverse and inclusive company culture that values individual perspectives and experiences. At Syneos Health, you will have the opportunity to work on cutting-edge projects and collaborate with a global team of passionate professionals who are dedicated to making a difference in the lives of patients. Join us in our mission to accelerate the delivery of therapies and bring positive changes to healthcare worldwide. For more information about Syneos Health, visit http://www.syneoshealth.com.,

As a Senior Clinical Operations Specialist (Senior CTA) in the Hybrid model in Athens at Syneos Health, you will play a crucial role in ensuring compliance with Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. Your responsibilities will include assisting Clinical Monitoring staff with site management activities, maintaining project files, handling project correspondence, participating in file audits, and preparing and maintaining site manuals and reference tools. Additionally, you will be responsible for updating clinical tracking information into databases, tracking documents, managing the shared mailbox, and coordinating site supplies and materials. You will collaborate with sites on assigned studies, communicate with them to ensure compliance with protocol requirements and relevant guidelines, and serve as a Sponsor representative. Your role will also involve anticipating, identifying, and resolving potential issues, implementing corrective actions, and seeking guidance as needed for more complex matters. Furthermore, you will participate in team meetings, prepare accurate meeting minutes and action items, and maintain awareness of clinical research by completing all necessary training. To excel in this role, you should preferably have an Associate's degree or equivalent experience in clinical research, pharma, biotech, or a related field. Good knowledge of medical terminology, clinical data, and ICH/GCP is preferred. You should possess strong organizational skills, attention to detail, and the ability to prioritize and work on multiple tasks. Excellent communication, presentation, and interpersonal skills are essential, along with the willingness to embrace new technologies. Minimal travel of up to 10% may be required as part of your responsibilities. At Syneos Health, we are committed to developing our employees through career progression, supportive line management, training programs, peer recognition, and a total rewards program. Our Total Self culture encourages authenticity and fosters a sense of belonging among our diverse workforce. By joining us, you will become part of a team dedicated to accelerating the delivery of therapies and changing lives. Syneos Health has a strong track record, having worked on a significant number of FDA-approved drugs, EMA authorized products, and numerous studies across various sites and trial patients. In our dynamic and competitive environment, you will be empowered to challenge the status quo and drive innovation. If you are passionate about making a difference in the field of clinical research and are looking for a challenging yet rewarding opportunity, consider joining Syneos Health. Learn more about us at http://www.syneoshealth.com.,