Senior Clinical Programmer (Rave+ Custom Function)

Description

Senior Clinical Programmer (Rave+ Custom Function)

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health
. 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. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
. We are continuously building the company we all want to work for and our customers want to work with. Why Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

• Programming and testing database design and implementation, ensuring data integrity and compliance with regulatory standards
• Coordinating business reporting for regional or transnational use, including the development and maintenance of reporting tools and dashboards
• Providing technical expertise to data management teams, offering guidance on best practices and troubleshooting complex issues
• Offering technical expertise to internal and external clients, including the preparation and presentation of technical documentation and reports
• Contributing to the design, implementation, and delivery of processes, programs, and policies, ensuring alignment with organizational goals and objectives
• Managing processes and programs, potentially directing the work of lower-level professionals, and ensuring timely and accurate completion of tasks
• Ensuring efficient and effective execution of technical aspects of clinical programming, including the development and validation of programming code and algorithms
• Collaborating with cross-functional teams to ensure data integrity and compliance, including participation in project meetings and providing input on technical aspects of clinical programming
• Developing and maintaining documentation for database design and implementation, including standard operating procedures and technical manuals
• Troubleshooting and resolving technical issues related to clinical programming, including the identification and implementation of corrective actions

Qualifications

• Bachelor's degree in Computer Science, Information Technology, or related field
• 5+ years of experience in iMedidata Rave Clinical Programming that includes basic and advance Study buildup activities, eCRF Design, Edit Check Programming, System Migration.
• Good experience with Custom Function Programming.
• Excellent Communication Skills
• Proficiency in programming languages such as SQL, SAS, or R
• Strong understanding of database design and implementation
• Excellent problem-solving and analytical skills
• Ability to work independently and as part of a team
• Strong communication and interpersonal skills

Certifications

• Certified Clinical Data Manager (CCDM) or equivalent certification preferred
• SAS Certified Professional or equivalent certification preferred

Necessary Skills

• In-depth knowledge of clinical programming and database design
• Ability to manage multiple projects and prioritize tasks effectively
• Strong attention to detail and accuracy
• Ability to provide technical expertise and guidance to team members
• Proficiency in data management and reporting tools
• Understanding of regulatory requirements and compliance standards

Get to know Syneos Health

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. Learn more about Syneos Health.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The 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 Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing 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 comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Summary

Roles within Clinical Programming job family at the P22 level are responsible for programming and testing database design, implementation, and business reporting. This includes planning and coordinating database design, implementation, and business reporting for regional or transnational use. These roles provide technical expertise to data management teams and offer technical expertise to internal and external clients. Impact and Contribution Roles within Clinical Programming job family at the P22 level contribute significantly to the design, implementation, and delivery of processes, programs, and policies. They use their in-depth knowledge and skills within the professional discipline to understand the impact of their work on related areas. These roles may be responsible for entire projects or processes within their area of responsibility, ensuring that the technical aspects of clinical programming are executed efficiently and effectively. Core Focus . Programming and testing database design and implementation . Coordinating business reporting for regional or transnational use . Providing technical expertise to data management teams . Offering technical expertise to internal and external clients . Contributing to the design, implementation, and delivery of processes, programs, and policies . Managing processes and programs, potentially directing the work of lower-level professionals . Ensuring efficient and effective execution of technical aspects of clinical programming