Clinical Programmer Analyst
at Adecco Canada
Nepean, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 11 Oct, 2024 | Not Specified | 11 Jul, 2024 | N/A | Data Analysis,Graphs,Bioinformatics,Creativity,Study Reports,Analytical Skills,Statistics,Data Science,Sql,Thinking Skills,Computer Science,Json,R,Sdtm,Regulatory Submissions | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Adecco is a hiring a Clinical Programmer Analyst for their client in Ottawa West. This is a one year contract role based onsite in Ottawa, Monday-Friday 8am-5pm.
- Location: Ottawa, ON
- Shift: Monday - Friday
- Job type: Temporary | Full-time
Responsibilities:
- Generate and validate tables, listings, and figures (TLF) based on specifications provided by Statistics and/or Clinical Writers.
- With minimal manager oversight, performs all data analytics activities for assigned studies.
- Ensures that all data analytics activities for assigned studies are completed on time and with high quality or escalates as appropriate.
- May support EDC development and visualization tools (PowerBI).
- Communicates well with peers, study teams and management as appropriate to support studies and goals.
- Represents the Data Analytics group at study team meetings.
- Applies best practices and established standards.
- Has a general understanding of the clinical trial process and regulations that apply.
- Seeks continuing education on latest in clinical and data science.
- Follows departmental Standard Operating Procedures (SOPs), and guidelines.
- Trains and mentors junior staff.
- Additional study specific activities.
Required Education and Experience:
- Must be eligible to work and reside within Canada.
- Minimum 3-5 years in a programming role.
- Bachelor’s Degree (Data Science, Computer Science, Statistics, Bioinformatics or relateddiscipline)
- Independently Develop SAS/R programs to generate and validate statistical output reports of trial data based on the SAP and TLFs mock-up shells
- Experience generating outputs for regulatory submissions (FDA, Health Canada)
- Programming experience in R, SQL, JSON
- Provide statistical programming support to Clinical Study Reports, data analysis an reporting
- Develop SAS/R programs to generate data listings, summary tables, and graphs for ongoing data cleaning and scientific data surveillance reviews
- Experience with CDISC and SDTM implementation desirable
- Support development of technical programming specifications for SDTM, ADS or ADaM standards.
- Knowledge of EDC development and visualization tools (PowerBI, Tableau) is an asset.
- Excellent Communications skills, both oral and written.
- Analytical skills, creativity and innovative approach to problem solving.
- Ability to collaborate effectively with multidisciplinary team members and also to work independently.
- Propensity for continuous learning and experimentation.
- Demonstrated initiative and problem-solving skills, critical thinking skills.
Are you interested in this position? Apply now! Our dynamic team of recruiters will reach out if you qualify for this role.
@@j
Responsibilities:
Adecco is a hiring a Clinical Programmer Analyst for their client in Ottawa West. This is a one year contract role based onsite in Ottawa, Monday-Friday 8am-5pm.
- Location: Ottawa, ON
- Shift: Monday - Friday
- Job type: Temporary | Full-tim
Responsibilities:
- Generate and validate tables, listings, and figures (TLF) based on specifications provided by Statistics and/or Clinical Writers.
- With minimal manager oversight, performs all data analytics activities for assigned studies.
- Ensures that all data analytics activities for assigned studies are completed on time and with high quality or escalates as appropriate.
- May support EDC development and visualization tools (PowerBI).
- Communicates well with peers, study teams and management as appropriate to support studies and goals.
- Represents the Data Analytics group at study team meetings.
- Applies best practices and established standards.
- Has a general understanding of the clinical trial process and regulations that apply.
- Seeks continuing education on latest in clinical and data science.
- Follows departmental Standard Operating Procedures (SOPs), and guidelines.
- Trains and mentors junior staff.
- Additional study specific activities
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Clinical Pharmacy
Graduate
Computer Science, Statistics
Proficient
1
Nepean, ON, Canada