Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.

Associate Director/Director, Strategy, Real World Evidence, Late Phase

DirectorDirectorFull TimeRemoteSeniorTeam 10,001+H1B SponsorCompany Site LinkedIn

Location

North Carolina

Posted

99 days ago

Salary

Not specified

Seniority

Senior

Bachelor Degree5 yrs expExperience acceptedEnglish

Job Description

• Act as a SME in RW study design and strategy across Syneos Health • Develop innovative Real World Data (RWD)-based solutions • Enhance growth, identify opportunities, and drive sales for the RWLP Business Unit • Work with current and potential clients to identify their RWE needs • Serve as liaison between sponsor and internal Syneos teams • Work closely with RWLP operations teams to determine project delivery requirements • Ensure customer satisfaction post-delivery • Work closely with Business Development to identify and generate early engagement and potential sales opportunities • Document all contacts in Salesforce for tracking and metrics • Provide accountability, preparation and leadership for customer ballparks, RFIs, RFPs, presentations • Analyze department sales data and overall opportunities and present to leadership • Represent Syneos Health by attending industry meetings, speaking engagements, participating in booth exhibitions • Identify and oversee the delivery of RWLP vendor/partner services

Job Requirements

BA/BS in the life sciences, nursing degree, or equivalent education or equivalent related experience
PhD preferred
Strong methodologic background across various RW study designs and methods
Strong RWD background and knowledge of US and ex-US RWD sources
Background in senior-level role in pharma or CRO preferred
Must have spent some time actively managing clinical and RW research projects across functional areas
Thorough knowledge of Regulatory requirements and the clinical development process
Flexibility to mentor and manage new staff
Minimum of five (5) to seven (7) years of RWLP Experience in a CRO, pharmaceutical, or Biotechnology Company