RWE Internship
at IQVIA
Oeiras, Área Metropolitana de Lisboa, Portugal -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Communication Skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Job Overview: We are seeking a motivated and detail-oriented Real-World Evidence (RWE) Intern to provide support for our clinical trials and evidence projects. This role offers a unique opportunity to gain hands-on experience in observational studies, monitoring tasks, and start-up activities, including the management of ethics committees and contracts with centers.
TEAM DESCRIPTION:
You will be joining a dynamic and collaborative team dedicated to advancing clinical research through real-world evidence. Our team consists of experienced professionals in clinical trials, medical writing, and project management, all committed to supporting your growth and development.
QUALIFICATIONS:
- Currently pursuing a Bachelor’s or Master’s Degree.
- Strong verbal and written communication skills suitable for a professional work environment.
- Demonstrated problem-solving, analytical, and critical thinking abilities.
- Proficiency in tasks aligned with the role’s requirements.
- Proven ability to work effectively in a team and communicate clearly.
CONTRACT DETAILS:
- This is a 12-month internship contract.
- Remuneration and meal allowances are provided.
- We are looking for someone who can start in December or January
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.co
Responsibilities:
- Assist in the execution of observational studies, including monitoring tasks.
- Support start-up activities such as managing ethics committees and coordinating contracts with centers.
- Provide support in medical writing tasks, including drafting protocols, Case Report Forms (CRFs), and other related materials.
- Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment
- Report for assigned Sponsors’ studies, as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a monthly basis per SSAE16 Controls
- Responsible to accurately complete all necessary journal entries as assign
- Responsible to quality review CTA and Payment Intake form setups to determine appropriate SAP vendor and payment method for Payments staff for assigned Sponsor’s studies, inclusive of bank entry validation for the Accounting dept.
- Responsible for SharePoint tracker completion for assigned sponsors.
- On an annual basis, assist with 1099 and other country tax reporting as assigned
- Special projects involving maintenance of the vendor database in SAP, and SOP Maintenance
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Proficient
1
Oeiras, Portugal