Clinical Programmer III India
Clinical Programmer III India
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
We are seeking a skilled SAS Clinical Programmer III with experience in SAS and EDC programming to join our dynamic team. In this role you will leverage your expertise in SAS programming and clinical data management to support the analysis and reporting of clinical trial data. Your contributions will be pivotal in ensuring the accuracy and integrity of our clinical databases
At Allucent we are dedicated to helping smallmedium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring lifechanging therapies to patients in need across the globe.
About the role
You will lead and coordinate clinical programming activities and maintaining clinical databases and other application tools supporting data capture and data processing in compliance with studyspecific plans standard operating procedures industry standards and regulatory requirements.
You will be part of a small but nimble global team. Credibility quality and collaborations are the key pillars that drive this team. We are looking for you to come with an innovative and candoapproach were you can have a quick impact.
Your main responsibilities will include but not limited to:
Data Management:
- Design build test and release clinical databases to the production environment including study design specifications Users Acceptance Test (UAT) test cases and database configuration settings in support of database setup 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 setup
- Support application of Clinical Data Interchange Standards Consortium (CDISC) conventions during database build activities and data warehousing i.e. CDASH TAUGs and SDTM models
- Review and adhere to the requirements of studyspecific data management documents & plans
Collaboration:
- 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 selftraining attending training classes professional meetings etc.
- Research and propose initiatives for improving efficiency
- Develops and delivers applicable DM departmental trainings
Quality Management:
- 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
This role is based in India where we have offices in Bangalore and Chennai and we are looking for someone that can come in the office at a minimum of 2 days a week.
Requirements
About you
You bring a minimum of 25 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 ICHGCP(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 handson 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 fastpaced challenging environment of a growing company.
Benefits
About Allucent
Our mission is to help bring new therapies to light. When you work at Allucent that means rolling up your sleeves and applying your unique skill set expertise and knowledge to build partnerships with our clients in their pursuit to develop new lifeimproving treatments.
If youre passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science business and operations leaders we would love to get to learn more about how we can help each other grow.
Together we SHINE. Find more information about our values.
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/inoffice 2 days a week)* 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 softskills 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
Apply now!
If you are interested in this role please apply through the button or for more information reach out to Yael Kokernoot
Disclaimers:
*Officebased employees are required to work inoffice no less than two 2 days per each work week. There are certain positions for which employees are required to work inoffice no less than three 3 days per each work week for employees within reasonable distance from one of ourglobal offices.
The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively Allucent). Allucent does not accept unsolicited resumes from thirdparty recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any thirdparty recruitment agency. Candidates should never be submitted directly to our hiring managers employees or human resources.
Employment Type
Full-Time
