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Project Manager - RTSM

extra holidays - extra parental leave - fully flexible

Remote:

Full Remote

Contract:

Full time

Work from:

Croatia

Offer summary

Qualifications:

Four-year degree or equivalent experience, Two+ years of Project Management experience within the Clinical Trial Industry, Superior organizational and communication skills, Working Knowledge Microsoft Office.

Key responsabilities:

Review protocols and draft User Requirements Specification (URS)
Manage deliverables like timelines, URS, system set up for RTSM projects
Ensure timelines are met and address system issues when needed
Provide technical support to internal teams like developers and customer support

Veeva Systems Computer Software / SaaS SME https://www.veeva.com/

5001 - 10000 Employees

See more Veeva Systems offers

Job description

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.

At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.

Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

Veeva Systems is looking for a Project Manager to join our Randomization & Trial Supply Management (RTSM) team. As a Project Manager, you will be the primary point of contact with the client, including leading client meetings and training sessions and highlighting the RTMS modules, which will deliver an effective, user-friendly RTSM system for end-users included in the study. Exceptional writing, editing/formatting, organization, and time management skills are a must.

What You'll Do

Review protocols and include required modules in the User Requirements Specification (URS)
Perform highly skilled duties such as creating, reviewing, coordinating, and managing a variety of deliverables (including, but not limited to, timelines, KOM, URS, Communication Manual, Requirements for Subject Randomizations, and Clinical Trial Material Lists for assigned projects, User Acceptance Testing, and system set up)
Ensure established timelines are met
Facilitate and troubleshoot any issues associated with managing the delivery of RTMS systems
Provide technical advice and assistance to other project managers, developers, validation, and customer support staff
Responsible for Tier 3 on-call coverage (24/7/365)
Acquire new knowledge and enhance your skills

Requirements

Four-year degree or equivalent experience
Two+ years of Project Management experience within the Clinical Trial Industry
Ability to take the initiative and work proactively
Superior organizational and communication skills
Working Knowledge Microsoft Office
Proven ability to work independently in a dynamic, fast-moving environment but also as part of a team
A logical approach to problem-solving and an excellent eye for detail
Excellent verbal and written communication, interpersonal, and presentation skills
Ability to travel (~5-10%)

Nice to Have

Working Knowledge of RTSM/IRT/IVRS/IWRS/IXRS
Working Knowledge of FDA E6, E8, and 21 CFR Part 11
Working Knowledge of Subject Randomizations and Clinical Trial Material lists
Audit Preparedness
Google Docs

#RemoteCroatia

Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.