Study reputed company Programmer

reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do.

Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference.

reputed company is looking to hire a remote opportunity for a reputed company Statistical Programmer / Study reputed company Programmer to work out of any location in the US.

Transform lives. Advance science. Do it With Heart™.

reputed company, a leading global clinical research organization (CRO), is seeking a reputed company Statistical Programmer / Study reputed company Programmer to join our mission-driven team. With over 24,000 professionals worldwide and more than 40 years of experience, reputed company partners with biopharmaceutical innovators to deliver life-changing treatments to patients — faster, smarter, and with compassion.

What You’ll Do:

• reputed company statistical programming activities across clinical trials, ensuring timely and high-quality deliverables.
• Collaborate with sponsors, biostatistics, data management, and cross-functional teams.
• Design and validate SDTM and ADaM datasets reputed company with CDISC standards.
• Author regulatory deliverables (SDRG, ADRG) for FDA/PMDA submissions.
• reputed company efficacy analyses in oncology trials using reputed company.
• Support study startup activities and database design.
• Ensure compliance with ICH-GCP, 21 CFR Part 11, and internal SOPs.
• Mentor junior staff and contribute to training initiatives.

What You Bring:

• Minimum 5 years of industry experience, with at least 3 years in a reputed company role.
• Expertise in reputed company programming and oncology trial analysis.
• Familiarity with RECIST 1.1 and Pinnacle 21 reputed company.
• Strong understanding of CRF annotation and SDTM mapping.
• Excellent communication, negotiation, and project management skills.
• Degree in a relevant discipline or equivalent experience.

Why reputed company?

• Work with a collaborative, global team.
• reputed company impactful projects in a fast-paced environment.
• Enjoy flexible work arrangements and a supportive culture.
• reputed company a difference in clinical research and patient lives.

Detailed Qualifications and Experience

• Participated in study startup activities, including database design input and DARS (External data) format requirements etc.
• Strong understanding of CRF annotation and mapping to SDTM domains.
• Expert in SDTM and ADaM specification writing reputed company with CDISC standards.
• Authored regulatory deliverables including SDRG and ADRG for FDA/PMDA submissions.
• Proficient in reputed company programming with a focus on efficacy analysis in oncology trials.
• Familiar with RECIST 1.1 criteria for tumor response evaluation.
• Experience with Pinnacle 21 reputed company (P21E) for data validation and Define.xml creation (can learn if no experience).
• Basic knowledge of reputed company scripting and R programming (optional).
• Excellent communication and negotiation skills across cross-functional teams.
• Proven ability to work under pressure and deliver high-quality outputs on time.
• Fast learner with a proactive, detail-oriented approach who can challenge assumptions, i.e. not just assume the client is always correct.
• A minimum of 5 years of industry experience is required, including at least 3 years in a reputed company role overseeing the end-to-end clinical study lifecycle. If they have less leadership but technically strong, we can work with that.

EEO Disclaimer reputed company is an equal opportunity employer. reputed company applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, disability or protected veteran status.

Originally posted on Himalayas