Join Clario as a Lead, Clinical Data Programmer in India

Are you an experienced Clinical Data Programming professional seeking an opportunity with an industry-leading data technology organization in the clinical research space? Clario is looking for a Lead, Clinical Data Programmer to join our well-established team in India. You'll work alongside a global team of data specialists to provide best-in-class data, supporting the development of life-changing therapies from clinical trials.

What We Offer

• Competitive compensation + commission scheme
• Attractive benefits to ensure security, flexibility, support, and well-being
• Engaging employee programs
• Technology for hybrid working and excellent onsite facilities

Your Responsibilities

• Lead and mentor a team of Clinical Data Programmers
• Create and test SAS code for standard and non-standard data file creation
• Review Clario standard and non-standard data specifications
• Attend client meetings to understand data collection requirements
• Review and finalize data specifications with Data Managers
• Develop programs for standard and non-standard data files
• Participate in the validation of encoding programs
• Perform ad-hoc programming activities based on requests
• Review User Requirements and create/approve Functional and Technical Specifications
• Provide programming support for DM activities
• Participate in internal and external audits
• Represent the service line through the NPI process
• Identify and implement methodological improvements
• Develop best practices to enhance quality, efficiency, and effectiveness
• Drive client deliverables and organize team resources
• Oversee training and development of Clinical Data Programmers
• Review and develop SOPs and associated documents
• Complete administrative tasks within Clinical Data Programming
• Participate in new hire interviews and provide feedback

Qualifications

• BS/BA Degree in Life Sciences, Computer Sciences, or related field preferred
• SAS ADVANCED certified
• At least five years of experience in a pharmaceutical company or CRO as a SAS Programmer
• Experience with SAS/BASE, SAS/MACRO, SAS/SQL products, and database design
• Understanding of the pharmaceutical drug development process
• Strong organizational, analytical, and communication skills
• Detail-oriented with extensive experience in implementing CDISC SDTM standards
• Proficient in Windows and Microsoft Office products
• Fluency in English (spoken and written)
• Knowledge of technical and regulatory requirements related to the role
• Excellent time management skills
• Proven leadership and mentoring skills
• Experience with large, complex real-world data sets a plus

Why Clario?

At Clario, we put people first. We are united and driven by our commitment to making a difference for patients. We are constantly innovating technology to shape the future of clinical trials and are always on the lookout for top talent to join our mission. It's through our dedicated people that we continue to transform lives.

EEO Statement

Clario is an Equal Opportunity Employer. We evaluate qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity, protected veteran status, disability, or any other legally protected characteristic.

Company Name: Clario

Job Title: Lead, Clinical Data Programmer