Patient Engagement Strategy Lead

Biogen
Full time Full day
Cambridge, MA

Job Description




As our Patient Engagement Strategy Lead you will be the key contributor to the accuracy of early program and study planning by developing and supporting processes related to patient recruitment and retention, patient and site input into Biogen protocols, protocol feasibility and investigator meetings across all GCO studies. 


Accountability


Patient Recruitment & Retention 



  • Support program and study teams by providing input and guidance regarding recruitment and retention (R&R) vendor engagement; leverage experience to ensure R&R vendor provides sound plans for recruitment and retention of patients; ensures R&R vendor is trained on Biogen processes and requirements

  • Provide continuity and connectivity between existing program/study feasibility efforts and development of recruitment and retention plans by R&R vendor

  • Support overall study planning by confirming R&R vendor is leveraging feasibility outputs, patient input and other available information when developing patient recruitment and retention strategy

  • Ensure R&R vendor incorporates MOA findings into country-specific recruitment & retention plans

  • Support the COS/COL by identifying issues, barriers, etc., to successful recruitment and retention of patients and confirm these are addressed by the R&R vendor early in strategy development

  • Direct R&R vendors and team members regarding efficient and timely review of recruitment & retention materials

  • Support the COL and QCPM by advising as to the internal process for engaging R&R vendor in delivery of study-specific strategic and tactical plans for recruitment and retention

  • Lead process improvement across the R&R space; provide ongoing assessment and input regarding quality of deliverables and performance of R&R vendors; assure strong R&R vendor support


Patient & Site Input into Biogen Protocols  



  • Identify & manage vendor(s) and develop process to support study teams regarding the assessment and incorporation of patient input into Biogen protocols to influence study design and early operational strategy with the goal of generating data to support executable, patient-friendly study designs and assessments

  • Collaborate with COLs to advise on options for gathering of feasibility data and to manage the process

  • Integrate FERO efforts with Biogen Advocacy to identify Patient Advocacy Groups who can provide patient/caregiver input/perspective on study design and study burden; develop methods to assess patient and site burden of schedule of assessments e.g., duration of visits, frequency of visits compared to SOC, questionnaire volume / survey fatigue, etc. 

  • Ensure CRO Partnership standard processes are evaluated and implemented (e.g., patient journey, etc.)

  • Collaborate with site/patient engagement efforts in the Clinical Country Management group


Protocol Feasibility



  • Evaluate opportunities for improvements in study feasibility process across studies within the CRO Partnership model (e.g., competitive landscape, country & site allocation plan, etc.); ensures the data and processes utilized for study start-up and enrollment plans from partner and other external vendors are effective

  • Ensure CRO Partnership study teams have optimal feasibility processes and data to inform decisions and plans

  • Evaluate if additional sources of information outside of the CRO Partnership should be incorporated into the standard process

  • Investigator Meeting Support

  • Lead process development for interface with preferred vendor for investigator meetings across GCO studies

  • Evaluate innovative approaches to investigator meeting content delivery and support COL in implementation of viable options

  • Evaluate and champion maximizing efficiency within the CRO Partnership for quality and consistency of logistics




Qualifications




  • Approximately 8 years of clinical research / project management experience including clinical site and CRO or sponsor experience

  • B.A. or B.Sc. in a scientific discipline; advanced degree preferred. Scientifically and clinically astute with very strong project management and communication skills



Additional Information



All your information will be kept confidential according to EEO guidelines.

This job is expired. Please use the search form to find active jobs or submit your resume.


Post a resume

Similar jobs

The Role: Join Moderna's enthusiastic and collaborative team and make a significant impact on the overall success of our innovative messenger RNA drug development programs. By joining our Pharmacovigilance team, the Associate Director/Director Pharmacovigilance Operations will provide critical PV quality...
Cambridge, MA
SAGE Therapeutics
Full time Full day
SAGE Therapeutics is searching for a patient-inspired, results oriented and collaborative sales professional with a proven track record in the acute and outpatient setting. The ideal candidate will have deep experience working with a wide range of customers to promote...
Cambridge, MA
Company Description Job Description Biogen's Pharmaceutical Operations & Technology (PO&T) Gene Therapy Department is searching for an individual to act as a technical leader for the Cell Culture Development group. The candidate will be expected to collaborate with other groups...
Cambridge, MA
MicroTasks.io

Want to take classes online or need someone to deliver food?

All from the comfort of your home.

LEARN MORE