Lead, Trial Delivery Manager
11 ore fa
Milan, Lombardy, Italia
Johnson & Johnson
Tempo pieno
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At Johnson & Johnson, we believe health is everything.
Controlli attentamente tutta la documentazione richiesta per la candidatura prima di fare clic sul pulsante apposito in fondo a questa descrizione.
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 .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.
We provide an inclusive work environment where each person is considered as an individual.
At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function: R&D OperationsJob Sub Function: Clinical Trial Project ManagementJob Category:ProfessionalAll Job Posting Locations:Madrid, Spain, Milano, Italy, Warsaw, Masovian, PolandJob Description:Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at We are searching for the best talent for a Lead, Trial Delivery Manager (TDM) to be located in one of the following locations (Hybrid or Remote working will be considered, depending on location and on a case-by-case basis).
Madrid, SpainMilan, ItalyWarsaw, PolandPosition Summary:The Lead Trial Delivery Manager (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 Lead 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.
You will be responsible for:Creating and updating critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
Managing vendor set up and management of day-to-day study vendor activities, including set-up, 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 country-level risk reviews, aware of all projects conducted across countries).
Supporting development of program-level compound training, collaborating with Clinical / CTL&D / Medical writing.
Providing input into trial level operational strategies.
Resolving trial-related issues and mitigate trial-related risks.
Participate in process improvement activities at a trial, compound & cross-DU level, as needed.
Providing support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues.
Mentoring & supporting onboarding of new team members, particularly those in Trial Management.
Principal Relationships:Internal: Trial Management Directors, Clinical Trial Leaders, Clinical Trial Assistants, Representatives of Delivery Operations, representatives of other GD Functions and Clinical Teams, representatives of Procurement External:Travel up to 15-20% of the time, defined by business needs.
Are you ready to join our team? Then please read furtherEducation and Experience RequirementsBS degree or equivalent, preferred areas of study include Life Sciences (Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)Minimum of 4 years clinical trial experience in Pharmaceutical, Healthcare or related industriesClinical research operational knowledge and experience across multiple phases of studies (Phase I-IV); must have the ability to manage multiple aspects of execution of a clinical trial.2-3 years’ experience supporting multiple aspects of a global clinical trial.
Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness.
Experience leading without authority and in muti-functional matrixed and global environments.
Excellent decision-making, analytical and strong financial management skills are essential to this position.
Operate and execute with limited supervision.
Experience mentoring/coaching others.
Ability to support and participate in the hiring, training, development, and evaluation of staff on a regular basis.
Strong project planning/management, communication and presentation skills are required.
Benefits:
We offer
a competitive salary and extensive
Controlli attentamente tutta la documentazione richiesta per la candidatura prima di fare clic sul pulsante apposito in fondo a questa descrizione.
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 .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.
We provide an inclusive work environment where each person is considered as an individual.
At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function: R&D OperationsJob Sub Function: Clinical Trial Project ManagementJob Category:ProfessionalAll Job Posting Locations:Madrid, Spain, Milano, Italy, Warsaw, Masovian, PolandJob Description:Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at We are searching for the best talent for a Lead, Trial Delivery Manager (TDM) to be located in one of the following locations (Hybrid or Remote working will be considered, depending on location and on a case-by-case basis).
Madrid, SpainMilan, ItalyWarsaw, PolandPosition Summary:The Lead Trial Delivery Manager (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 Lead 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.
You will be responsible for:Creating and updating critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
Managing vendor set up and management of day-to-day study vendor activities, including set-up, 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 country-level risk reviews, aware of all projects conducted across countries).
Supporting development of program-level compound training, collaborating with Clinical / CTL&D / Medical writing.
Providing input into trial level operational strategies.
Resolving trial-related issues and mitigate trial-related risks.
Participate in process improvement activities at a trial, compound & cross-DU level, as needed.
Providing support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues.
Mentoring & supporting onboarding of new team members, particularly those in Trial Management.
Principal Relationships:Internal: Trial Management Directors, Clinical Trial Leaders, Clinical Trial Assistants, Representatives of Delivery Operations, representatives of other GD Functions and Clinical Teams, representatives of Procurement External:Travel up to 15-20% of the time, defined by business needs.
Are you ready to join our team? Then please read furtherEducation and Experience RequirementsBS degree or equivalent, preferred areas of study include Life Sciences (Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)Minimum of 4 years clinical trial experience in Pharmaceutical, Healthcare or related industriesClinical research operational knowledge and experience across multiple phases of studies (Phase I-IV); must have the ability to manage multiple aspects of execution of a clinical trial.2-3 years’ experience supporting multiple aspects of a global clinical trial.
Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness.
Experience leading without authority and in muti-functional matrixed and global environments.
Excellent decision-making, analytical and strong financial management skills are essential to this position.
Operate and execute with limited supervision.
Experience mentoring/coaching others.
Ability to support and participate in the hiring, training, development, and evaluation of staff on a regular basis.
Strong project planning/management, communication and presentation skills are required.
Benefits:
We offer
a competitive salary and extensive