Job description:-

We are seeking a skilled Clinical SAS Programmer with expertise in SDTM, ADaM (Safety and Efficacy) , and TLFs to join our team. The ideal candidate must also have hands-on experience or knowledge of R programming.

Location: Ridgefield, CT, United States
Job Type: Contract 1 years with possibility of extension

Key Responsibilities::
•Remote Position but must come onsite in Ridgefield, CT for a week for on-boarding and training.
•Part time role with 20-30 hour per week but must be flexible on work hours as they will be working with Germany team. (More morning hours as they will be working with Germany team)
Its more Technical writing role in regulatory submissions. RA Associate will do but must have technical writing experience.
•Understating of how SOPs work in regulatory submissions .
•Ability to ask and clarify questions to SME’s
•Ability to meet deadlines.
•Proficient in MS office and Adobe PDF
•Strong documentation experience. Keeping track of documents for Dept. and SMEs
•Previous admin experience necessary. Steady work history needed.

Required Qualifications::
• Minimum Bachelor degree required with 4 – 5 years experience.

How to Apply:

If you meet the above qualifications and are interested in joining our team, please send your resume to pc_mentriix@hscrp.net.