Clinical Research Sas Programmer

WHY VITALIEF?

Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees.  If you are interested in a rewarding career path, a healthier “Life” work balance, and working with a team that respects and encourages your voice, then we want to speak with you!

Vitalief, a fast-growing, “best of breed” Research Operations and Clinical Trials Consulting Company, is committed to identifying talented and passionate Clinical Research professionals to join our exceptional team and support our clients in planning and executing successful clinical trials.

Advantages of working at Vitalief:

• Ability to have a voice challenging the status quo with novel thinking
• Transparent Leadership
• Investment in your career progression
• Employee incentive/reward program
• Encouraged and mentored by the talented Vitalief team to achieve full potential
• 20 PTO (Paid Time Off) days plus 9 paid Holidays annually
• Other benefits include:Company paid life insurance and short / long term disability coverage; 401K retirement program; Robust healthcare plans to choose from

Location:  Home-based with some optional domestic and/or international travel.  Candidate must live in NY, NJ, PA or DE to be considered for this position.

Salary Range:  $75K - $90K annually (depending on experience level)

Overview:

Under the direction of the Director of Research Operations and Principal Investigator, the Data Programmer Analyst is responsible for statistical programming, technical support, and data management oversight of protocols within an NIH Consortium conducting research on infectious diseases (TB, HIV, COVID-19). Sites based domestic and international across a variety of designs - prospective, retrospective, electronic health records and other formats will collect and provide data to Rutgers University hosting the Data Resource Core for this Consortium. Data Programmer Analyst will provide advanced programming skills, as it relates to data management of specific protocols – including implementing data capture/management, developing databases, harmonizing databases of various studies/mixed platforms and establishing quality control SOPs, conducting periodic quality assurance monitoring, work with investigators to develop and implement protocols at the international sites. Develops and maintains appropriate electronic databases consistent with protocol aims and works with Clinical Science Core staff and investigator(s) on data management needs customized to each protocol.

Responsibilities:

• Provides leadership and training to international site staff in programing REDCap case report forms (CRFs) and databases consistent with approved protocol(s) to capture clinical and laboratory data.
• Designs and develops complex statistical programs for research data cleaning, transfer, and analysis.
• Implements coding scripts to automate large data validation checks.
• Provides innovative solutions to issues pertaining to large clinical and bio-repository database capturing and quality management.
• Implement new technologies and software (i.e., FreezerPro, Freezerworks) to maintain biorepositories and other databases for various research studies.
• Implements scripts to facilitate integration of different databases.
• Facilitates, coordinates instruments administration, data gathering software and data collection.
• Develops systems and SOPs for monitoring the quality of data quality for each protocol.
• Develops materials to assist with training of data management staff to maintain electronic data capture system (REDCap), develops CRFs, program validation checks of data.
• Completes all documentation and paperwork in a timely and efficient manner.

Required Skills:

• Bachelor’s Degree, in Public Health, Biomedical Informatics, or related sciences plus 2+ years of statistical programming experience.
• Master’s Degree is a plus.
• Advanced proficiency with SAS programming language.
• Intermediate experience with statistical packages and programming languages such as MS Excel, R, MS Access, etc.).
• Good understanding of Clinical Research components - data collection, human subjects’ protection, quality assurance and control.
• Strong computer knowledge and graphic experience a plus.
• Ability to learn and integrate other related computer applications into existing operations. Ability to program in various languages to create, harmonize and set up for analysis various databases.
• Must have excellent project management, time management, communication, interpersonal, decision making, analytic, and reporting skills.
• Must be able to work with a wide range of individuals with diverse backgrounds and perspectives on data usage including faculty, staff, and senior administrators, as well as individuals at other institutions and government offices.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 25lbs.

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

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