Clinical Programmer Iii

**In this role your key tasks will include**:

- Design, build, test and release clinical databases to the production environment, including study design specifications, User’s Acceptance Test (UAT) test cases and database configuration settings in support of database set-up and edit checks programming. You will work with SAS and EDC programming.
- Review electronic Case Report Form (eCRF) Completion guidelines
- Develop and/ or validate SAS programs for metric reporting, data review listings, data import and data export set-up
- Review and adhere to the requirements of study-specific data management documents & plans
- Actively contribute/participate in study team, departmental meetings, sponsor meetings and uses analytical approach to problem solving
- Collaborate with peers, programmers, study teams to clarify specifications and uses expanded technical skills to meet evolving project needs
- Maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading literatures, self-training, attending training classes, professional meetings etc.
- Research and propose initiatives for improving efficiency
- Develops and delivers applicable DM departmental trainings
- Draft and contribute as Subject Matter Expert (SME) in the field of Clinical Programming activities to the evaluation/improvement of processes and procedures within the Quality Management System

**Requirements**:
**To be successful you will possess**:
You bring a minimum of 2-5 years of relevant work experience in a clinical research and/or drug development organization combined with a degree in Life science and experience in SAS and EDC programming. Computer Science, healthcare and/or related field degree. You will be a great addition to the team when you are open and transparent, work well together and have a solution focused approach.
- To be successful we are looking for the following traits and behaviors: _
- Good knowledge of ICH-GCP(R2), GDPR/HIPPA and applicable (local) regulatory requirements.
- Good understanding of clinical data management processes and experience with tools and systems for managing clinical studies.
- Solid understanding and hands-on experience with CDISC standards (i.e. CDASH, TAUGs and SDTM models).
- Strong programming SAS skills with proficiency in Electronic Data Capture (EDC) systems, data reporting and programming languages such as PL/SQL, SAS and comparable fields.
- Ability to work in a fast-paced challenging environment of a growing company.

**Benefits**

**Benefits of working at Allucent include**:

- Comprehensive benefits package per location
- Competitive salaries per location
- Departmental Study/Training Budget for furthering professional development
- Flexible Working hours (within reason)
- Opportunity for remote/office-based* working depending on location
- Leadership and mentoring opportunities
- Participation in our enriching Buddy Program as a new or existing employee
- Internal growth opportunities and career progression
- Financially rewarding internal employee referral program
- Access to online soft-skills and technical training via GoodHabitz and internal platforms
- Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
- Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

**Disclaimers**:

- Office-based employees are required to work in-office no less than two (2) days per each work week. There are certain positions for which employees are required to work in-office no less than three (3) days per each work week for employees within reasonable distance from one of our global offices.