Site Activation Partner Jobs

· 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:

Strong leadership and organizational management skills, ability to exercise sound judgment and make decisions independently and proactively identify and solve problems

Minimum of 3 years CRO/pharmaceutical industry experience, preferably in Start-up Management, Project Management, and/or Site Management experience

Lead and manage assigned SA project teams to achieve successful delivery of milestone achievements and any key performance indicators

Ability to provide experience and input into initiatives relating to interacting with sites and/or customer

Strong oral and written communication skills to clearly and concisely present information

Team-oriented work style; seeks and gives guidance

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:

School diploma/certificate with equivalent combination of education, training and experience; BS/BA or bachelor’s degree in life sciences preferred

Manage and coordinate with other supporting roles to ensure timely site activation and operational activities.

Support global initiatives as it pertains to the role and responsibilities

Minimum 4 years relevant experience in Clinical Trials environment, Ethics environment and clinical site activation.

Experience working in the pharmaceutical industry or CRO in a similar role

Demonstrated deep knowledge of clinical trial methodologies, ICH/GCP, Global and local country regulations

Commitment to ongoing education to meet resident’s needs and legislative requirements.

Facilitates, as assigned, Residents’ Council activities in accordance with legislative requirements.

Experience in long term care in developing/ leading programs for residents with varied physical and cognitive ability.

Experience in PCC and Activity pro would be considered as an asset.

Knowledge of community resources within the service area and able to relate to them in a professional manner.

As an Activation Manager, you will be accountable for:

Commitment to ongoing education to meet resident’s needs and legislative requirements.

Facilitates, as assigned, Residents’ Council activities in accordance with legislative requirements.

Experience in long term care in developing/ leading programs for residents with varied physical and cognitive ability.

Experience in PCC and Activity pro would be considered as an asset.

Knowledge of community resources within the service area and able to relate to them in a professional manner.

As an Activation Manager, you will be accountable for:

If this opportunity matches your qualifications and experience, please apply on-line.

Attend in-service education sessions, staff meetings, workshops, etc. as directed by the Supervisor, Resident Support Services

Activation Therapist responsibilities as per job description

Must have a valid CPR/First Aid certification

Must possess teaching skills to convey techniques to guide residents and families

Must have organizational skills to prioritize work and coordinate scheduling with other members of the health care team

2 years relevant experience in clinical site management

Experience in study activation and site management is an asset

Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

Demonstrated knowledge of global and local regulatory requirements

Must have Study Start up experience

Minimum of 2 years of related experience

Knowledge of website content management software

Professional skills and experience required:

Assessment and monitoring of the local patient experience

At least three (3) years of experience in a similar role

Plan and deploy the integration marketing plans of each local clinic in their portfolio

Ensure the compliance and accuracy of the newsletters of the clinics in their charge

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:

2 years relevant experience in clinical site management

Experience in study activation and site management is an asset

Minimum of 2 years of related experience

Experience with PC-Windows, word processing, and electronic spreadsheets required.

Knowledge of ICH and local regulatory authority drug research and development regulations is required.

Clinical trials support or pharmaceutical industry experience required.