Sr Programmer Analyst - Pharmacovigilance
at Thermo Fisher Scientific
North Carolina, North Carolina, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 12 Feb, 2025 | Not Specified | 12 Nov, 2024 | 5 year(s) or above | Sql,Programming Languages,Perspectives,Computer Science,Timelines,Sas,Information Technology,Training | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
TRIAL PROGRAMMER SPECIALIST III
Are you ready to join a team that strives for outstanding and flawless execution in every project? At Thermo Fisher Scientific, we are looking for an ambitious Trial Programmer Specialist III to become part of our world-class information technology team. This is an outstanding opportunity to contribute to groundbreaking projects and compete at the highest levels of the industry.
KNOWLEDGE, SKILLS AND ABILITIES:
- Proven experience as a programmer in a clinical trial setting.
- Strong knowledge of programming languages such as SAS, SQL, and R.
- Outstanding analytical and problem-solving abilities.
- Ability to strictly adhere to timelines and project deadlines.
- Excellent communication and collaboration skills.
- Bachelor’s degree in Computer Science, Information Technology, or a related field; equivalent experience will also be considered. Advanced degree is preferred.
- Demonstrated success in developing and implementing programming solutions in a regulated environment.
Thermo Fisher Scientific Inc. offers an inclusive and collaborative work environment that values a diverse group of backgrounds and perspectives. Join us and contribute to implementing innovative solutions that have a real impact in the world
Responsibilities:
KEY RESPONSIBILITIES:
- Design, develop, and implement trial programming solutions to support clinical trials.
- Collaborate with cross-functional teams to determine programming requirements and deliverables.
- Ensure data integrity and compliance with regulatory requirements.
- Develop and maintain documentation related to trial programming processes.
- Conduct rigorous testing and debugging to ensure the flawless operation of programs.
- Provide technical support and training to junior programmers and other team members.
- Contribute to the establishment and adoption of programming standards and effective practices.
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Information Technology/IT
IT Software - Other
Software Engineering
Graduate
Proficient
1
North Carolina, USA