Senior Clinical Data Science Lead

at  ICON

Home Based, KwaZulu-Natal, South Africa -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate19 Jan, 2025Not Specified20 Oct, 2024N/AGood communication skillsNoNo
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:

As a Senior Clinical Data Science Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
You will be joining a well-established team fully outsourced to one of our global pharmaceutical clients. You will be responsible for ensuring overall successful development, implementation and maintenance of the Data Management actvities of phase 1-4 clinical trials on either a global or regional level.
Reporting to the Senior Manager of Data Management and working as part of the global Data Management team, you will have oversight of the data management project deliverables and serve as the leader for the Study Management Team. You will manage and track key study metrics to ensure adherence to data management milestones.

WHAT ICON CAN OFFER YOU:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We’re proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
https://careers.iconplc.com/reasonable-accommodations
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles

Responsibilities:

  • Developing, implementing and maintaining the Data Management Plan
  • Execution of data validation plans
  • Reporting on the status of projects and tasks
  • Proposing solutions to process and technical issues
  • Ensuring timely generation and tracking of data queries
  • Interacting with the sites, CRA’s and Lead CDC’s
  • Reconciliation of external data

You are:

  • Degree qualified with demonstrable experience working within a CRO and or pharmaceutical industry
  • Proficiency in at least one Clinical Data Management system required
  • Experience with all steps within the Data Management lifecycle from setup to maintenance and database lock
  • Experience as primary representative of Clinical Data Management project team
  • Proven history of successful interaction with internal and external clients and an understanding of related functions
  • Communication skills and an ability to quickly build relationships


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Clinical Pharmacy

Graduate

Proficient

1

Home Based, South Africa