20 bästa jobben som fraud i stockholm (Rekryterar nu!)

Snr CRA
IQVIA —Stockholm
- Heltid
- Microsoft Word
- Microsoft Excel
- Engelska
8d
Swedish speaking Customer Support Agent in Malta
Next Job Abroad —Stockholm
- Heltid
- Engelska
- Kontor
- Gymkort
Ansök direkt
Integrationsutvecklare - Tieto Tech Consulting (m/f/d)
Tieto —Solna
- Heltid
- Bankväsende
- Python
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Accountable Lead, Workforce Management - Fincrime Operations
Klarna Bank AB —Stockholm
- Heltid
- Ledarskap
- Livförsäkring
Swedish-speaking Customer Support Agent for iGaming Company in Malta
Next Job Abroad —Stockholm
- Heltid
Ansök direkt
Head of Operational Excellence, Tieto Indtech
Tietoevry —Solna
- Heltid
- Ledarskap
- Kommunikationsfärdigheter
1d
Sales Manager - Tieto Tech Consulting (m/f/d)
Tietoevry —Stockholm
- Heltid
- Försäljning
- Engelska
- Kommunikationsfärdigheter
Senior Customer Manager Public 360°- Tieto Indtech (m/f/d)
Tietoevry —Solna
- Heltid
- CRM-program
- Försäljning
- Engelska
1d
Data Engagement Partner – Banking (Sweden/Nordics)
LTM —Stockholm
- Försäljning
- Praktik
Ansök direkt
Overseas Contractor
LTM —Stockholm
- Heltid
- Engelska
- Databaser
- Analytisk förmåga
Ansök direkt
Senior FinCrime Analyst
Alchemy Group —Stockholm
- 40 000SEK - 52 000SEK per månad
- Heltid
- Analytisk förmåga
- Kommunikationsfärdigheter
Ansök direkt
Senior Machine Learning Engineer
Rebtel —Stockholm
- Engelska
- Kontor
- Masterexamen
- Gymkort
Delivery Solution Architect – Hybrid Cloud, Infrastructure & AI Solutions
Hewlett Packard Enterprise —Stockholm
- Heltid
- Engelska
- Windows
- Linux
Product Manager Energy Information Exchange (EIX) - Tieto Indtech (m/f/d)
Tietoevry —Solna
- Heltid
- Engelska
- Ledarskap
AI/ML Engineer
RebTel Networks AB —Stockholm
- Heltid
- Engelska
- Kontor
- Masterexamen
- Gymkort
Senior Robotic Startup Specialist
Medtronic —Stockholm
- 554 400SEK - 831 600SEK per år
- Heltid
- Engelska
- Kandidatexamen
2d
Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)
IQVIA —Stockholm
- Heltid
- Engelska
- Forskning
- Business development
DevOps Engineer - Tieto Caretech (m/f/d)
Tietoevry —Solna
- 3 800SEK - 6 000SEK per månad
- Heltid
- Python
Head of Operational Excellence, Tieto Indtech
Tieto —Solna
- Heltid
- Ledarskap
- Kommunikationsfärdigheter
Ansök direkt
1d
Head of Sales, Credit & Wealth - Tieto Banktech (m/f/d)
Tietoevry —Solna
- Heltid
- Försäljning
- Engelska
- Ledarskap
4 tim

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Snr CRA

IQVIA -
Stockholm

Ansök nu

Jobbinformation

Heltid
8 dagar sedan

Kvalifikationer

Microsoft Word
Microsoft Excel
Engelska
Kandidatexamen
Organisationsförmåga
Kommunikationsfärdigheter

Fullständig jobbeskrivning

Stockholm, Sweden | Full time | Home-based | R1564231

Job Overview

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

This is part of the multi-sponsor team and requires experience working on Oncology trials.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.

Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.

Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Act as a mentor for clinical staff including conducting co-monitoring and training visits.

Collaborate and liaise with study team members for project execution support as appropriate.

If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.

If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree in scientific discipline or health care preferred.

Requires at least 4 years of year of on-site monitoring experience.

Equivalent combination of education, training and experience may be accepted in lieu of degree.

In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Strong therapeutic and protocol knowledge as provided in company training.

Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).

Written and verbal communication skills including good command of English language.

Organizational and problem-solving skills.

Effective time and financial management skills.

Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

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.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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Jag vill få den senaste jobbevakningen för fraud i stockholm

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