Manager, Trial Delivery Management

2 months ago

Titusville, Florida, United States tapwage Full time
Johnson and Johnson is currently seeking a Manager, Trial Delivery Management . This position can be located remotely within the United States.

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at [])


For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.

Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.


We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve.

Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.


The Manager, Trial Delivery Management (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, vendor oversight & delivery, compound training, and other activities.

The TDM is responsible for country and regional oversight of local operational delivery, including the alignment of the feasibility strategy and target setting, risk reviews and local challenges that could impact overall study delivery.


Primary responsibilities:

  • Create and update critical trialspecific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation)
  • Vendor set up and management of daytoday study vendor activities, including setup, SOW creation and budget oversight
  • Responsible for country / regional coordination of trial management activities and oversight (e.g., aligns feasibility strategy with local teams, perform countrylevel risk reviews, aware of all projects conducted across countries)
  • Support development of programlevel compound training, collaborating with Clinical / CTL&D Medical writing
  • Provide input into trial level operational strategies
  • Resolve trialrelated issues and mitigate trialrelated risks
  • Participate in process improvement activities at a trial, compound & crossDU level, as needed
  • Provide support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues
  • Mentor & support onboarding of new team members, particularly those in Trial Management

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