Senior Manager, Site Engagement, Sponsor Dedicated
ICON Clinical Research, LP
West Coast, US
Site oversight & delivery activities
Establish and manage site relationships
Develop and implement a plan to raise company profile
Establish and manage site relationships, acting as a liaison between the company and investigational sites, building investigator and site staff awareness on client compounds
Job Summary
Establish and manage site relationships, acting as a liaison between the company and investigational sites, building investigator and site staff awareness on client compounds.
Develop and implement a plan to raise the profile of the company and its global clinical development projects with current and potential investigators.
Oversee site-level study start-up, conduct, and close-out activities outsourced to CRO(s) for global programs across Therapeutic Areas.
Matching Summary
Establish and manage site relationships, acting as a liaison between the company and investigational sites, building investigator and site staff awareness on client compounds.
Skills & Requirements
Must-have
Site Oversight & Delivery Activities
Establish and manage site relationships
Develop and implement a plan to raise company profile
Evaluate investigational sites
Work with Medical/Patient/Industry Associations
Knowledge of site capabilities and past performance
Ensure regular communication with local organization
Oversee site-level study start-up, conduct, and close-out
Support Site Agreement negotiations
Identify trends, issues and risks across sites
Ensure sites are activated in a timely manner
Ensure sites deliver on expected recruitment targets
Ensure ICH/GCP/local regulatory requirements are observed
Provide documented sponsor site oversight
Utilize site performance and quality data
Strong communication skills (verbal, written and listening)
Ability to work independently
Sound negotiation skills
Record of vendor interactions
Sound critical thinking skills
Detail-oriented, organized and committed to quality
Results driven and capable of managing competing assignments
Proven track record of achieving deliverables
Ability to work in a dynamic environment
Ability to communicate effectively with KOLs, site staff, and internal team members
Nice-to-have
Oncology and/or Neurology and/or Immunology TA experience desired
Experience and proven proficiency in CTMS and eTMF systems preferred
Key Requirements
Substantial (8+ years) experience in clinical operations
Graduate background (Medical or Life Sciences degree) or equivalent