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Clinical Project Manager

Employer
Formation Bio
Location
Working from home
Start date
Sep 28, 2021

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Job Details

About TrialSpark

The biggest bottleneck in bringing new treatments to patients is the clinical trial. On average, getting a drug through the trial process takes nearly a decade and frequently costs $1B+. And the problem is only getting worse.

TrialSpark finds new medicines and develops them cheaper and faster, using our proprietary trial engine.

Position Overview

As a Clinical Project Manager, you will play a key role in the execution of TrialSpark’s full study offering. We are looking for an experienced project manager who can execute our Project Management strategy and deliver fast, high quality studies. As part of your role, you’ll partner closely with other leaders across the company, contributing to TrialSpark’s broader Clinical Trial Engine strategy and build out. 

Duties and Responsibilities

Duties include but are not limited to: 

Key responsibilities will include:

  • Using industry knowledge, experience, and first-principles thinking to refine our strategy for delivering key study services, with a primary focus on Project Management.
  • Leading execution of TrialSpark’s initial portfolio of POC, Phase II, and real-world evidence studies, including oversight of trial performance, management of vendors, and leadership of cross-functional study teams.
  • Developing clinical trial timelines and budgets, and ensuring study teams deliver against time, quality, and cost targets.
  • Partnering with cross-functional teams from Operations, Data Management, Medical, Engineering, QA, and more to develop capabilities.
  • Represent TrialSpark to study sponsors, including driving reporting and updates, where appropriate.
  • Lend industry expertise across TrialSpark, helping us plot our route toward making clinical trials faster, more efficient, and higher quality.

About you

Skills, abilities, and knowledge

  • Critical thinker with the ability to step back and rethink legacy assumptions in the clinical research space; should be able to point to what’s wrong, and how you would do it differently if starting from scratch.
  • Excellent cross-functional partnership skills; you know how to work across an organization to achieve objectives and meet timelines.
  • Superior written and oral communication skills; can synthesize complex concepts and deliver messages clearly.
  • Competency with data analysis: should have intermediate+ ability with Excel, and fluency with managing to metrics and key performance indicators.

Education and Experience

  • 5+ years clinical research industry experience
  • 3+ years of clinical project management experience at a biopharma company or CRO 
  • BS required, preferably in life sciences or a related field; advanced degree preferred

You will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Company

Formation Bio is a tech-driven pharma company differentiated by radically more efficient drug development. Formation Bio has built a technology platform that optimizes all aspects of drug development, enabling more efficient trial design, faster trial completion, and higher quality trial data capture.

Formation Bio acquires clinical-stage drugs from pharma and biotech and develops them faster and more efficiently, unlocking greater value per program and accelerating access to new treatments for patients.

Join our culture of innovation where your work directly contributes to transforming patient care in areas such as rheumatology, dermatology, CNS, and cardiometabolic diseases. Our dynamic environment blends advanced technology with strategic drug development, speeding up the delivery of new treatments. Here, every role plays a part in our mission to bring new treatments to patients faster and more efficiently.

Company info
Website
Phone
+1 510-545-3803
Location
16 East 34th Street floor 10
New York
NY
10016
United States

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