Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation. 

Job Title: Associate Project Manager

Location: Ontario, Canada (Hybrid Work Model)

Function: Service Delivery

ESSENTIAL DUTIES AND RESPONSIBILITIES:

·      Assist in the creation, ongoing management and closeout of databases of Sitero’s eClinical projects, by working closely with the Data Management Team and team members

·      Project Planning / Timelines

o  Support in the coordination of key documents that define study timelines and responsibilities

o  Assist in the tracking of study timelines and deliverables

·      Coordination and support of internal / client meetings

o  Web-based and in-person meeting support

o  Development of meeting support materials (Minutes, Actions)

·      External Communication

o  Prepare draft communication in a timely and effective manner with the Client, Vendors and Sites

·      Support Sitero’s application support:

o  eCRF/Module Configuration

o  eCRF/Module Validation/Testing

o  Validation of Sitero’s outputs ie. Reports, Data Listings, SAS, etc.

o  Sitero’s eClinical Suite deployment support and build testing

o  Development of eCRF related tools, including: Source Documents, Study Completion Guidelines and Tips & Tools / User Guides 

o  Issue Management: Work with the Project and Customer Care Teams to respond to project-related end-user inquiries

EDUCATION AND EXPERIENCE REQUIRED:

·      Bachelors Degree required

·      Clinical Research Postgraduate Certificate preferred

·      Knowledge of ICH-GCP required

·      Experience with EDC systems strongly preferred

·      1+ years of experience with a pharmaceutical manufacturer, Biotech, or CRO required

COMPENSATION & BENEFITS:

Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, paid time off, and healthcare and retirement benefits.

EMPLOYMENT TYPE:

Full Time, Permanent

COMMITMENTS:

·      Standard Hours 40 hours per week, one hour lunch, Monday – Friday.  Additional hours as needed.

·      Willing to work in shifts as and when needed.

DISCLAIMER:

Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.