Job Title: Coordinator II, Clinical Data
Company: Abbott
Location: Delhi Cantonment, Delhi, India
Job Type: Full-time
Industry: Hospitals and Health Care
Education: An equivalent combination of education and work experience
Experience: Minimum 2 years
About the Company: Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals, and branded generic pharmaceuticals, Abbott serves people in more than 160 countries and employs approximately 109,000 people.
Job Description: As a Coordinator II, Clinical Data at Abbott, you will be working under general supervision to ensure the integrity of clinical data in the database. Your primary responsibility will involve reconciling images required by studies, captured at the site level, with images uploaded to a third-party image repository. You will issue queries to clinical sites for missing images, review query responses, and verify image uploads. Additionally, you will reconcile data between various platforms and assist in discrepancy management efforts. This role requires attention to detail, organizational skills, and the ability to work in a fast-paced environment.
Responsibilities:
- Reconcile images required by studies captured at the site level with images uploaded to a third-party image repository.
- Issue queries to clinical sites for missing images and review query responses.
- Reconcile data between various platforms including CRF data, third-party image platform, and corelab.
- Process incoming clinical data forms accurately and according to departmental processes.
- Support discrepancy management efforts by preparing data clarification forms.
- Identify and discuss problems in the area of clinical data coordination.
- Maintain the integrity of information stored in the clinical database.
- Provide support to the clinical evaluation department in preparation for on-site monitoring visits.
- Remain current on developments in the field of clinical data coordination.
Qualifications:
- Minimum 2 years of experience as a Clinical Data Coordinator or in a closely related clinical research environment.
- Demonstrated organizational skills and attention to detail.
- Ability to work under general supervision and handle multiple projects simultaneously.
- Strong interpersonal skills and ability to communicate effectively with stakeholders.
- Knowledge of FDA, Good Manufacturing Practices (GMP), and Good Clinical Practices (GCP) regulations.
- Ability to work in a fast-paced, changing environment and within a highly matrixed business environment.
- Minimal travel required.
