fbpx

Site Selection Coordinator


The Site Selection Coordinator provides support to the Site Selection Specialist and to project teams to identify and select sites to participate in clinical trials.

 

This role is perfect for you if:

  • You have an interest in working with clinical research sites;
  • You want to work in a collaborative environment;
  • You want to have an impact in a fast-growing company.

 

RESPONSIBILITIES

 

More specifically, the Site Selection Coordinator:

  • Develops and maintains positive and productive relationships with key clinical research sites.
  • Participates in the maintenance of the investigators database to support site identification and selection.
  • Participates in the identification of investigators and research sites to expand the investigator database and for clinical trials.
  • Contacts potential investigators identified for the project to confirm their interest in participating in clinical trials.
  • Coordinates the review and negotiation of the confidentiality agreement of the interested sites.
  • Coordinates the preparation, submission, and collection of feasibility questionnaires completed by the sites using the approved templates.
  • Coordinates the review of feasibility questionnaires completed by the sites.
  • Tracks key activities in CTMS.
  • Assists with regulatory filing.

IDEAL PROFILE

  • Bachelor's degree in a field relevant to clinical research or equivalent experience.
  • Experience in clinical research and in the biotechnology, pharmaceutical, and/or CRO industry, an asset;
  • Excellent oral and written skills in English, French is an asset;
  • Excellent knowledge of the Microsoft Office suite (i.e., Word, Excel, PowerPoint, Outlook).
  • Strong ability to carry out different projects simultaneously, to organize their work effectively, and to work under pressure in accordance with deadlines.
  • Good judgment and problem-solving skills.
  • Experience in customer service is an asset.
  • Strong interpersonal skills.
  • Good knowledge of good clinical practices, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines.

 The work environment

 At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities. 

 

In this position, you will be eligible for the following perks: 

  • Flexible work schedule
  • Permanent full-time position
  • Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities)
  • Offices near public transportation (Sherbrooke metro station or Saint-Laurent metro station)
  • Possibility of working from home in accordance with company policies and public health directives
  • Ongoing learning and development

 

 

 About Innovaderm

Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe. 

Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

 

Innovaderm only accepts applicants who can legally work in Canada.

All Available Positions


Position Department Location
Quality Assurance Specialist, Supplier Audits Quality Assurance Canada
Clinical Research Associate (CRA), Dermatology CRO - Clinical Monitoring Remote, Canada
Clinical Research Associate (CRA), Dermatology CRO - Clinical Monitoring Remote, Canada
Team Lead Patient Recruitment Clinical Site Montréal, Canada
Senior Manager, Vendor management CRO - Project Management Canada
Associate Project Manager CRO - Project Management Spain
Clinical Research Assistant (Part-Time) Clinical Research Unit Montreal, Canada
IT Technician (support Level 1) Corporate - Information Technology Montréal, Canada
Administrative Assistant Clinical Site Montréal, Canada
CRA Line Manager (Spain) CRO - Clinical Monitoring Spain
CRA Line Manager (Poland) CRO - Clinical Monitoring Poland
Strategist, Patient Recruitment and Site Engagement CRO - Project Management Montréal, Canada
Site Selection Coordinator CRO - Project Management Montreal, Canada
Senior Statistical SAS Programmer (India) CRO - Biometrics India
Senior Biostatistician (India) CRO - Biometrics India
Process Improvement Specialist Corporate - IT and Support Services Canada
Site Selection Specialist CRO - Project Management Canada
Associate Project Manager CRO - Project Management Poland
Associate Project Manager CRO - Project Management Canada
Senior Biostatistician CRO - Data Management and Statistics Canada
Vendor Manager CRO - Project Management Canada
Clinical Research Auxiliary Nurse Clinical Research Unit Montreal, Canada
Manager, eTMF Operations CRO - Regulatory and Scientific Affairs Montreal, Canada
CRA Manager CRO - Clinical Monitoring Montreal, Canada
Regulatory Affairs Coordinator CRO - Scientific and Regulatory Affairs Montréal, Canada
Project Coordinator (Clinical Research) CRO - Project Management Canada
Project Manager (Poland) CRO - Project Management Poland
Project Manager (Spain) CRO - Project Management Spain
Medical Monitor CRO - Regulatory and Scientific Affairs Poland
Proposal and Contract Manager Sales and Marketing Canada
Clinical Trial Manager CRO - Clinical Monitoring Home-based, Canada
Project Manager CRO - Project Management Canada
Budget and Contract Specialist CRO - Site Selection and Contracting Canada
Future opportunities General Montreal, Canada