Clinical Programmer Analyst

at  Adecco Canada

Nepean, ON, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate11 Oct, 2024Not Specified11 Jul, 2024N/AData Analysis,Graphs,Bioinformatics,Creativity,Study Reports,Analytical Skills,Statistics,Data Science,Sql,Thinking Skills,Computer Science,Json,R,Sdtm,Regulatory SubmissionsNoNo
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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.
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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