Site Lead Jobs in Quebec

· Management of roughly 25-30 sites in regulatory activation per FTE

What we look for (minimum qualifications):

· 2 years of clinical and 2+ year of experience in a clinical site activation environment

· Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

Benefits of Working in ICON:

Collection and submission of regulatory documents

Management of roughly 25-30 sites in regulatory activation per FTE

Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems

2 years of clinical and 2+ year of experience in a clinical site activation environment

Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

What we look for (minimum qualifications):

Benefits of Working in ICON:

Management of roughly 25-30 sites in regulatory activation per FTE

Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems

2 years of clinical and 1+ year of experience in a clinical site activation environment

Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

What we look for (minimum qualifications):

Benefits of Working in ICON:

Operate like Workplace Services is your business and your product; think like a product manager and a general manager

Exhibit strong analytical, conceptual thinking, strategic planning and execution skills. Be a proven creative thinker with a problem-solving approach

Have an evolving knowledge of commercial and corporate real estate with the willingness to become an expert

Has experience in working with multiple countries and cultures within the EMEA region.

Qualifications like NEBOSH, IFM, MCR, etc. are advantageous.

Assist to strategic planning for moves, adds, and changes (MAC) in coordination with space planning/occupancy

Post-secondary education in a Certified Medical Office Administration Program or similar experience working in a medical office environment.

Essential daily responsibilities and duties as a Medical Office Administrator (MOA) or Medical Assistant (MA) for the clinic.

Overseeing any schedule changes (Endocrinology, Diabetes Education Program, Chiropody, and any other departments as required).

Responsible for distributing work assignments if manager not at the site.

1-2 years leadership experience in a healthcare setting, preferred.

Proficient knowledge of Electronic Medical Records system (knowledge of Accuro, an asset).

Excellent verbal, written, communication and time management skills

Responsible for site identification related resource management for studies including, but not limited to:

Project-specific financial management including, but not limited to:

Communicating changes to resource requirements (change in scope) to LM’s and central resourcing team

Proactive in identifying scope creep & communicating to Site ID Manager & PL.

Experience working in a pharmaceutical, biotech, contract research organization or clinical research site

Management of roughly 25-30 sites in regulatory activation per FTE

Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems

2 years of clinical and 1+ year of experience in a clinical site activation environment

Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

Benefits of Working in ICON:

Initiate investigator site activities, including: