Cpl Life Sciences

HTA and Evidence Synthesis Manager

Location
Central London / West End
Posted
02 Jul 2021
Closes
31 Jul 2021
Ref
JO-2107-471738
Contact
Luke Sandilands
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

HTA and Evidence Synthesis Manager
12 Month Contract
Fully Remote
Day Rate Negotiable

Cpl Life Sciences are actively recruiting on behalf of one of our leading Pharmaceutical clients for an experienced HTA and Evidence Synthesis Manager

Responsibilities include:
- Executes economic models and outcome studies and consults with the Director on economic models
- Designs and executes existing data studies, Executes on Global Health Economics (GHE)-related aspects (e.g. PRO strategy) of observational studies and interventional trials and consults with the Director on their responsibilities in these tasks
- Executes on PRO strategy for observational studies and interventional trials and consults with the Director on their responsibilities in these tasks,
- Drafts GHE publications for dissemination and consults the Director and external collaborators? Contributes to the GHE component of the Global publication Plan and provides oversight and review of GHE component of publications prior to submission
- Drafts and executes the Value Evidence Generation Plan, GVD and GHE related sections of the Global Payer Plan, and GXP�s, Selects and works with study vendors, contracting liaisons, and tracks budgets.
- As directed, engages and manages relationships with Key Opinion Leaders (KOLs), industry experts, reimbursement advisors, etc. Works with Directors when necessary, to present to GPT, PST, TASC and CST Responsible for project level review at either IPRG, PRC or ORRG; Skills: Masters, PharmD, or PhD; health economic experience

If you're interested please send your CV to luke.sandilands@cpl.com or apply for this role. 

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