Feasibility Manager

Posted 7 Days Ago
Be an Early Applicant
Hiring Remotely in United States
Remote
97K-145K Annually
7+ Years Experience
Biotech
The Role
The Feasibility Manager in the Precision for Medicine team oversees the management and delivery of various feasibility projects related to clinical trials. They conduct pre-award and post-award analyses, support business development efforts, and ensure the quality and accuracy of feasibility data and processes throughout the project lifecycle. The role involves collaboration with operational strategy teams and client interactions to support successful trial execution.
Summary Generated by Built In

Position Summary: 

Feasibility Manager is a member of the expert team within Feasibility Department of Precision for Medicine. As part of this team, this role has responsibility for the management and delivery of pre-award, post-award, rescue, and stand-alone-feasibility projects. The Feasibility Manager leads pre-award feasibility projects and supports business development and operational strategy teams by conducting detailed feasibility analysis and presenting at internal and client meetings. The Feasibility Manager leads feasibility projects for newly awarded and/or ongoing clinical trials and supports start-up and clinical teams with site identification, study strategy(ies) and enrollment modeling. In addition, Feasibility Manager participates in specific projects that enables Precision for Medicine to stay at the forefront of innovation and maintain their competitive edge as a scientifically driven engaged partner for our biotech and pharma clients. 

Essential functions of the job include but are not limited to:  

  • Leading pre-award feasibility projects
  • Provide detailed pre-award support to operational strategy and business development teams:
  • Provide feasibility analysis and input for pre-award RFPs, including: competitive analysis, historical recruitment analysis, standards of care, drug analysis, epidemiology analysis, site and country analysis 
  • Provide enrollment modelling(s) for agreed study strategy(ies)  
  • Undertake feasibility site outreach for pre award opportunities
  • Support and/or attend BDM and client calls
  •  Apply process, templates and delivery standards for feasibility pre-awards
  • Leading post award feasibility projects
    • Provide guidance for post-award, rescue and standalone feasibility in alignment with study and client requirements
    • Manage feasibility project team in all aspects pertaining to the conduct of the feasibility:
    • Provide training and training materials
    • Ensure that feasibility project team is meeting agreed timelines and deliverables 
    • Ensure accuracy and quality of the survey data
    • Oversee and /or conduct the site outreach process.
    • Present feasibility strategy at KOM and provide regular updates to sponsor 
    • Where appropriate, engage with patient advocacy groups and site networks in order to support study feasibility, recruitment and successful delivery 
    • Conduct the analysis of the collected site data to provide accurate site identification, enrollment modeling and study strategy (ies)
    • Apply process, tracking, templates, data structure delivery standards for post award and stand-alone feasibility
  • Participate in growth of the Feasibility Department and Precision for Medicine:
  • Work closely with the Precision study teams to assess required input from the feasibility team, and agree on delivery plan, including roles and responsibilities, for feasibility pre and post-award 
  • Ensure that post and pre award feasibility process, SOPs templates and tools, are implemented and followed
  • Support development of feasibility process documents and SOPs 
  • Support Business Development in client meetings and bid defense presentation

Qualifications: 

Minimum required: 

  • A minimum of 7 years of related experience
  • A Bachelor’s degree in a life sciences discipline
  • Combination of qualifications and equivalent relevant experience may be accepted as an alternative

Other Required: 

  • Competence and relevant experience in the required activities for the role including feasibility analysis, site identification
  • Domestic and international travel including overnight stays up to 10% of time 
  • Ability to communicate both verbally and in writing at the English proficiently (Professional level). 

Preferred: 

  • Postgraduate degree preferred.

Skills 

  • Excellent  management and organizational skills
  • Strong oral and written communication skills in English
  • Strong rationale and analytical thinking
  • Established IT platform and data analysis skills
  • Active listening and strong presentation abilities
  • Able to collaborate with diverse stakeholders
  • Strong computer skills, specifically with MS Word, Excel, PowerPoint, and with web/data based platform

Competencies  

  • Strong sense of ownership and pride in quality of outputs 
  • Strong attention to detail
  • Team player with ability to work independently 
  • Willingness to work in a matrix environment, work independently and as part of a dynamic team 
  • Embraces the established Precision for Medicine’s Cultural Values as an underlying tenet to drive work behaviors
  • Demonstrates good knowledge of ICH-GCP, relevant Precision for Medicine’s SOPs and regulatory guidance, as well as the ability to implement such items.

 



Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case.  This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$96,500$144,700 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.


Top Skills

Life Sciences
The Company
HQ: Bethesda, MD
1,114 Employees
On-site Workplace

What We Do

Precision is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. This maximizes our clients’ insight into patient biology, delivering more predictable trial outcomes and accelerating clinical development. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.

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