Clinical Developer

• Build and maintain clinical trials for customers
• Collaborate with customers and internal resources to create accurate, complete and fully functional clinical trials
• Document study build requirements, changes, and overall project tasks and timelines
• Test clinical trials developed to ensure accuracy prior to moving into Quality Assurance
• Execute mid-study change requests to ensure project workflow is timely and accurate
• Maintain study fixes for all clinical trials based on Technical Support Services escalation processes
• Participate in Customer and Management meetings as needed
• Oversee Clinical Development as needed to resolve technical issues
• Troubleshoot incidents escalated to Clinical Development following Customer Care escalation processes
• Estimate and assign project tasks to ensure workload is properly managed and distributed across the team
• Work with stakeholders and customers to create and map requirements and convert them to reports
• Identify and map data and create new reports using SQL queries
• Develop software in compliance with industry regulations such as 21 CFR Part 11

• Ability to function in a highly collaborative, fast-paced team environment
• Excellent analytical skills with the ability to manage multiple priorities and requests
• Excellent communication and interpersonal skills
• Proven leadership experience to ensure proper guidance is provided to the Clinical Developers
• Expert problem solver with attention to detail
• Proficiency in Anju Software's clinical products, or the ability to quickly become proficient
• Ability to work independently in a fast-paced environment
• Excellent communication and documentation skills
• Strong work ethic and willingness to learn
• Excellent problem resolution follow-up skills to ensure all projects are handled in a timely manner
• Proven technical leadership in a team environment
• Bachelor's degree in a related field of study or related work experience
• Minimum of 4+ years of experience with DHTML (HTML + JavaScript)
• High-level understanding of SQL and IIS
• Solid project management skills
• Proven leadership skills
• Knowledge of clinical trial design and setup
• Understanding of GCP/ICH guidelines for the conduct of clinical trials
• Knowledge of FDA regulations and/or experience within the life sciences industry preferred

• Provident Fund (PF) contributions
• Medical and term insurance coverage, per company policy
• Paid time off: vacation, personal and sick leave, floating holidays and public holidays
• Reimbursement of approved work-related travel expenses