SCiAN Services Inc.

www.scian.com

1 Job

17 Employees

About the Company

SCiAN Services Inc., is a contract research organization (CRO) providing clinical data management, biostatistics, medical writing, SAE management and custom database solutions to the pharmaceutical, biotechnology, and medical device industries. SCiAN has its headquarters in Toronto, Ontario Canada. We are known in the industry for our client-oriented approach, high quality standards, response to time-sensitive deliverables and proactive/innovative problem-solving skills. SCiAN Services Inc. maintains the highest standards for value, quality, return on investment and support in all the services we provide: We invest in training our personnel and applying leading-edge technologies to the services we provide. We provide our clients with the knowledge and experience to ensure the success of every study and customize our approach to meet the individual needs of each client.

Listed Jobs

Company Name: SCiAN Services Inc.
Job Title: Clinical Data Associate II
Job Description: **Job Title** Clinical Data Associate II **Role Summary** Reviews and processes clinical trial data to maintain accuracy and consistency of clinical databases in alignment with study‐specific Clinical Data Management Plans (CDMP). **Expactations** - Deliver data management activities on time and to quality standards. - Collaborate with cross‑functional teams (project, database, audit) to resolve discrepancies and support user testing. - Maintain data integrity and comply with regulatory and internal audit requirements. - Operate effectively with moderate supervision and adapt to shifting priorities. **Key Responsibilities** - Interpret and follow study CDMPs. - Assist in compiling CDMP documentation. - Design and develop study databases from CRF templates. - Create and implement custom validation rules and checks. - Prepare and conduct database user testing and documentation. - Perform non‑medical data reviews per Clinical Data Validation Plans. - Manage discrepancy resolution workflow. - Verify database changes and update databases following queries or DCFs. - Prepare subject data files for audits and quality control activities. - Participate in study‑specific data entry training. - Provide clerical and administrative support to CDM and BST teams. - Support project managers with document tracking, scanning, and database audits. - Perform other assigned duties. **Required Skills** - Experience with clinical database systems (e.g., EDC, Lotus Notes). - Knowledge of data validation, edit checks, and database design. - Basic familiarity with SAS or other programming languages. - Understanding of medical terminology. - Strong written and verbal communication. - Ability to work independently and prioritize tasks. - Team‑oriented attitude and willingness to learn. **Required Education & Certifications** - Bachelor’s degree in Life Sciences, Biology, or related field (preferred). - Minimum 1‑2 years of experience in clinical database management. - No specific certifications required, but familiarity with ICH, FDA, or GLP guidelines is an asset.