Sponsor Dedicated CRA I
Location
Portugal
Posted
42 days ago
Salary
0
Seniority
Mid Level
No structured requirement data.
Job Description
Sponsor Dedicated CRA I
Syneos Health
Role Description Sponsor Dedicated CRA I - Home Based Portugal - Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms. - Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates. - Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials. - Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues. - Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans. - Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct. Qualifications - Bachelor's degree in a related field or equivalent experience. - Minimum of 1 year of experience in clinical research monitoring. - Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements. - Excellent communication and interpersonal skills. - Ability to work independently and manage multiple priorities. - Proficiency in using clinical trial management systems and other relevant software. - Location in Lisbon area will be preferred. Requirements - Attention to detail and strong analytical skills. - Problem-solving abilities and critical thinking. - Ability to work effectively in a team environment. - Strong organizational and time management skills. - Proficiency in Microsoft Office Suite. Benefits - We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. - We are committed to building an inclusive culture – where you can authentically be yourself. - We are continuously building the company we all want to work for and our customers want to work with. Company Description Over the past 5 years, we have worked with 94% of all 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 quo with us in a highly competitive and ever-changing environment.
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