Principal Portfolio Lead Clin Prog

at  Johnson Johnson

High Wycombe, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate17 Nov, 2024Not Specified21 Aug, 20245 year(s) or abovePython,Data Manipulation,Reporting,Data Structures,Programming Languages,R,Computer Science,Mathematics,SasNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Portfolio Lead, Clinical Programming
Johnson & Johnson are currently seeking a Portfolio Lead, Clinical Programming to join our Integrated Data Analytics & Reporting (IDAR) Department. This position is based in High Wycombe (Hybrid). Remote work options in the UK may be considered on a case-by-case basis and if approved by the company.
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 https:// www.jnj.com/.
Position Summary
As Portfolio Lead, Clinical Programming, this position is responsible for formulating the clinical programming strategy across a set of clinical trial and/or report activities, compound, disease, therapeutic or reporting group area, indication assigned of medium to high complexity. They are accountable for the effective planning and execution of programming activities across multiple clinical trials for their assigned portfolio ensuring effective partnership with, and management of stakeholders.
This position drives operational excellence, consistent implementation of data standards, program and report library templates and macros as programming lead. Accountable for effective resource allocation and utilization of resources as well as optimal assignment of work in accordance with sourcing decisions, people/ partnership development goals and business needs.
Additionally, they provide leadership and/or expertise in relevant technical areas and on process improvement, maintenance and innovation initiatives working proactively to connect with teams, peers and leadership within and cross functions, sharing and implementing lessons-learned and shaping processes and practices.

Role and Responsibilities

  • Accountable for clinical programming strategy across assigned portfolio of medium to high complexity, scope and/or criticality within compound, disease area, indication or Therapeutic Area.
  • Responsible for the planning, execution and completion clinical programming activities on time, within budget, and with high quality, consistent with departmental and company quality and compliance standards for assigned area.
  • Proactively evaluates and manages resource demand and allocation of internal and external team members to meet current and future business needs ensuring effective utilization of resources and maintenance of functional planning systems.
  • Collaborates effectively with team and cross-functional counterparts and vendors to achieve project goals.
  • Participates in hands on project or trial initiation activities, as needed.
  • Contributes to and/or leads departmental innovation and process improvement projects and development of disease or therapeutic area standards, training as required, may contribute programming expertise to cross functional projects/initiatives.
  • Ensures compliance of assigned teams and personnel with company and department SOP’s, policies and regulatory guidance documents.
  • The position mentors and coaches and delegates work.

QUALIFICATIONS

Requirements

  • Bachelor’s degree or higher and/or equivalent in computer science, data science/data engineering, mathematics or another relevant scientific field (or equivalent theoretical/technical depth). Advanced degree (Master’s, PhD or equivalent) preferred.
  • Approximately 8-10+ years clinical programming experience with increasing responsibility OR Masters/MBA in a relevant field and 6-8+ yrs. relevant experience OR PhD in a relevant field and 5+ yrs. relevant experience. Experience in a pharmaceutical/ clinical trial environment preferred.
  • Advanced knowledge of data structures and relevant programming languages for data manipulation and reporting. May include SAS, R, Python, etc. Knowledge of SAS is required.
  • Demonstrated project leadership experience managing risks, resources and leading teams to successful outcomes.
  • Strong communication, influencing and negotiation skills.

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

Responsibilities:

  • Accountable for clinical programming strategy across assigned portfolio of medium to high complexity, scope and/or criticality within compound, disease area, indication or Therapeutic Area.
  • Responsible for the planning, execution and completion clinical programming activities on time, within budget, and with high quality, consistent with departmental and company quality and compliance standards for assigned area.
  • Proactively evaluates and manages resource demand and allocation of internal and external team members to meet current and future business needs ensuring effective utilization of resources and maintenance of functional planning systems.
  • Collaborates effectively with team and cross-functional counterparts and vendors to achieve project goals.
  • Participates in hands on project or trial initiation activities, as needed.
  • Contributes to and/or leads departmental innovation and process improvement projects and development of disease or therapeutic area standards, training as required, may contribute programming expertise to cross functional projects/initiatives.
  • Ensures compliance of assigned teams and personnel with company and department SOP’s, policies and regulatory guidance documents.
  • The position mentors and coaches and delegates work


REQUIREMENT SUMMARY

Min:5.0Max:10.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Computer science data science/data engineering mathematics or another relevant scientific field (or equivalent theoretical/technical depth

Proficient

1

High Wycombe, United Kingdom