Job Posting: Clinical Data Associate II (Rave)
Company: Syneos Health
Location: Home-Based, India-Asia Pacific
Industry: Pharma/Healthcare/Clinical Research
Job ID: 24005135
Application Deadline: 30th October 2024
About Us
Syneos Health is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. We seamlessly connect our capabilities to add high-value insights that speed therapies to patients and provide practical value to help our customers achieve their objectives.
Position Overview
We are seeking a detail-oriented Clinical Data Associate II to join our team. In this role, you will be responsible for managing clinical data for assigned projects, ensuring compliance with study-specific Clinical Data Management Plans (CDMP), and performing User Acceptance Testing (UAT) among other critical tasks.
Key Responsibilities
- Maintain awareness of contract elements and scope of work for assigned projects.
- Review and adhere to study-specific Clinical Data Management Plans.
- Create and enter test data for User Acceptance Testing (UAT).
- Perform UAT for data entry screens and data review listings.
- Manage lab normal ranges and complete necessary access forms.
- Review discrepancy outputs and validation listings, applying corrections as needed.
- For paper studies, manage Data Clarification Forms (DCFs) and ensure all documentation is filed appropriately.
- Conduct internal quality checks for both electronic and paper studies.
- Participate in internal meetings and audits as required.
- Maintain proficiency in Data Management systems through ongoing training.
Candidate Profile
- Education: BA/BS degree in biological sciences or related fields.
- Experience: Preferred experience in data management practices and relational database management systems (Oracle Clinical, Rave, or Inform).
- Skills: Proficiency in MS Windows, Word, Excel; excellent communication and interpersonal skills; strong organizational and time management abilities.
- Knowledge: Familiarity with medical terminology and ICH/Good Clinical Practices is a plus.
- Attributes: Ability to multitask, work independently and as part of a team, adapt to changing priorities, and meet tight deadlines.
Additional Information
- Travel Requirements: Minimal travel may be required (up to 25%).
- Compliance: Responsible for adhering to Corporate Business Practices, Standard Operating Procedures, and other duties assigned by management.
If you are ready to contribute to the advancement of clinical research and enhance patient care, we encourage you to apply.