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Regulatory Affairs Consultant (Lithuania)

Employer
Parexel
Location
Lithuania
Salary
Competitive
Start date
17 Oct 2021
Closing date
14 Nov 2021

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Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Job Description

Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.

This role can be either office based in Vilniaus or you can be fully home based anywhere in Lithuania. The office is open planned, and you will be working in an innovative and collaborative environment connecting with colleagues from around the world.

As the Consultant you will have an understanding of the organization's consulting models and methodologies, as
well as, good knowledge of what services Parexel provide. You must have strong technical skills andalso be able to develop specialist knowledge of a particular subject and/ or market. You will ensure thetimely performance of work within a project scope to the quality expectations of the group and the client. Whenserving as a Project Lead or Work Stream Lead, you will also assure the work of the entire team or workstream is delivered on time and that it meets client's and PC's quality expectations.

Key Accountabilities:

Project Execution
- Typically works within a team environment but may work; independently delivering services within their technical area of; expertise;
- Works within broad project guidelines but liaises closely with more; senior colleagues to discuss issues and resolve conflicts
-Demonstrates ability to prioritize work and define steps needed to; achieve specified project outcomes

Consulting Activities and Relationship Management
- Follows and implements the organization's consulting models andmethodologies
- Provides technical and/or business consulting services within
personal area of expertise
- Completes assigned activities within project scope and objectives withan understanding of issues which may impact project profitability
- Collaborates with colleagues and client to identify and resolvetechnical and process issues

Business Development
- Continue to build a network of industry colleagues throughrelationships formed during project engagements or through otherindustry experience
- Communicates potential new business leads to PC management andaccount managers
- May participate in project scoping calls and/or proposal preparationwith the support of senior colleagues

Parexel related responsibilities
- Meets established metrics as specified in scorecard on an annual basis
- Completes basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, project deliverable archiving, participation in internal initiatives/projects or as a mentor as requested by managementQualifications

Education:
- Minimum of a Bachelor's Degree in a Scientific or Technical Discipline, Advanced Degree Preferred

Skills:
- High-level consulting skills
- Critical thinking and problem-solving skills
- Project leadership and management knowledge
- Excellent interpersonal and intercultural communication skills, both written and verbal
- Client-focused approach to work
- Results orientation
- Teamwork and collaboration skills
- Proficiency in local language and extensive working knowledge of the English language
- Networking
- Business analysis
- Self-confidence and control

Knowledge and Experience:
- Extensive experience in an industry-related environment; experience with a regulatory agency (such as FDA, MHRA) is a plus
- Previous CRO / Pharma experience acting in the capacity of a Regulatory Affairs Consultant or Senior Regulatory Affairs Consultant
- Client-focused approach to work (Quality)
- Regulatory Project Management/Lead experience

In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry. Your hard work will be rewarded with a competitive salary, bonus and benefits package including days holiday and other leading edge benefits that you would expect with a company of this type.

Apply today to begin your Parexel journey!Why Work at Parexel

There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?

That's Parexel. We're a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.

How can we help you on your journey? Find your path, and learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.

Company

parexel

When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there’s no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change – forever. And together, we’ll do it With Heart™.

How to describe Parexel’s culture in one word: 

Henry

 

 

Working With Heart™ - Christina's perspective:

Working With Heart™ - Christina's perspective:

 

Careers Blog | Our Culture | Diversity, Equity & Inclusion | Benefits | Our Hiring Process

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. 

Company info
Website
Telephone
+44 1895 238000
Location
The Quays
101-105 Oxford Road
Uxbridge
Middx
UB8 1LZ
United Kingdom

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