Clinical Programmer

Clinical Programmer

• →Support the clinical programming lead on project teams, and serve as lead programming lead, as needed.
• →Program standard and study specific electronic Case Report Forms (eCRFs), edit checks and reports.
• →Set-up study specific mapping for WHO-Drug and MedDRA dictionaries.
• →Ensure the efficiency, quality, and integrity of database development, reporting and project activities.
• →Perform data checks as needed to ensure integrity and correctness of data displays and to understand structure and content of data.
• →Perform QC/validation of vendor datasets, clinical data listings and edit checks to verify the output.
• →Perform other duties as assigned.
• →Interact across operational areas as required.
• →Interact with sponsor representatives as required

• A minimum of 2 years of relevant work experience, including programming experience with Clinical Database Management Systems, i.e., Medidata Rave, Medrio, IBM, etc.; SAS programming experience also preferred.

• Previous experience in pharmaceutical research or a CRO setting preferred.
• A satisfactory combination of education and experience may be accepted as a substitute for the specific education and experience listed above.

Required Certifications:  N/A

Required Skills:

• Excellent verbal, written, and interpersonal skills.
• Knowledge of clinical trial study design.
• Able to work on multiple, concurrent projects.
• A high degree of accuracy and attention to detail.
• Can attend study team meetings as needed.

• Ability to travel for meetings or training activities may be required.
• Strong organizational, problem-solving, and analytical skills.
• Versatility, flexibility, and a willingness to work within constantly changing priorities.
• Commitment to excellence and high standards.