Clarivate BSc, MSc Life Sciences Clinical & Regulatory Consultant Recruitment, Apply Online

Clarivate Clinical & Regulatory Consultant Recruitment For BSc, MSc Life Sciences, Apply Online

Clarivate Clinical & Regulatory Consultant Recruitment For BSc, MSc Life Sciences, Apply Online. MSc & BSc Life Sciences Job. Apply online for the Clinical and Regulatory Consultant vacancy at Clarivate. Interested and eligible applicants can check out all of the details on the same below:

Hey there, if you are interested in this role of Clinical and Regulatory Consultant
at Clarivate then make sure you check out some interview questions along with their answers that we have listed at the bottom of the page

Job Title: Clinical and Regulatory Consultant

Job Number: JREQ121518

City, ST: Bangalore, KA

The Regulatory Solutions Consultant is a member of Life Sciences Consulting Services team; reporting directly to the Manager, Regulatory Consulting Services. The primary purpose of the Regulatory Solutions Consultant role is to support the proposal and delivery of regulatory consulting services globally. This includes working closely with the Manager, Regulatory Services and other team members to ensure that all regulatory projects are delivered on time, within cost and at the highest quality.

This is a great opportunity to increase your background and lead several different Regulatory Intelligence projects related with

clinical trials, marketing authorization applications (MAA), chemistry manufacturing and controls (CMC), CMC variations, pharmacovigilance projects, and regulatory strategy, among others. We work with companies with portfolios that include both chemical and biologics, as well as Medical Devices and Invitro Diagnostics. With this role you will support global clients on their challenges when operating globally, providing regulatory intelligence support and helping them to be more efficient and strategic.

About You – experience, education, skills, and accomplishments 

• Minimum of a Bachelor’s degree in life sciences or Master’s degree in life sciences
• Knowledge of pharmaceutical and medical device regulatory affairs / regulatory intelligence across a given geographic area (e.g. Europe or North America) mandatory (familiar with drug pipeline, development / approval / marketing, regulatory concepts).
• Experience in supporting regulatory professional services or projects desirable.
• Customer facing or customer service experience desirable.

It would be great if you also had . . . 

• Expert knowledge in key areas of responsibility e.g. operating systems, networking technologies, security standards
• Relevant experience in clinical trial data optimization, clinical data management, MAA submissions
• Regulatory Intelligence – Pharmacovigilance, Clinical Trial, New and post approval registrations, etc.
• Strong problem management, troubleshooting and analytical skills
• Demonstrated ability to work with and manage virtual teams to successfully deliver projects
• Demonstrated ability to learn and understand internal systems and processes

What will you be doing in this role?

Project Delivery Support (90%)

• Become an integral member of the delivery team within the Life Sciences Consulting group.
• Act as a point of contact for the customer throughout a project’s lifecycle.
• Act as the project manager for regulatory professional services to ensure successful delivery of each assigned project; which includes coordination and tracking.
• Escalate any project risks and delivery issues to the Manager, Regulatory Services for action and resolution.
• Support and delivers small pilot projects to validate understanding between the proposed solution and customer needs identified during the sales process.
• Support the delivery of non-regulatory professional services as required and agreed with both their direct and matrix managers.
• Deliver on routine projects and single requests.

Business development (10%)

• Support to any received Requests for Information (RFIs) and Requests for Proposals (RFPs).
• Work with professional services colleagues to provide robust effort estimates for scoped projects.
• Support the creation of customer facing materials to support commercial discussions such as samples.

Hours of Work 

This role is full-time and will be part of a fast-paced global team working with colleagues in varying time zones and regions where collaboration, creativity and ingenuity are encouraged.  12pm to 9pm IST Flex

At Clarivate, we are committed to providing equal employment opportunities for all persons with respect to hiring, compensation, promotion, training and other terms, conditions and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.

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We know you are here all eager and wanting all of the answers, so read on below to read and absorb some of the interview questions for the role of Clinical and Regulatory Consultant at Clarivate

1. Can you explain your experience and knowledge of pharmaceutical and medical device regulatory affairs across a specific geographic area? Answer: In my previous role, I gained extensive experience in pharmaceutical and medical device regulatory affairs across Europe. I am familiar with the drug pipeline, development, approval, marketing processes, as well as regulatory concepts. I have worked on projects involving clinical trials, marketing authorization applications (MAA), chemistry manufacturing and controls (CMC), CMC variations, and pharmacovigilance. This experience has allowed me to navigate the regulatory landscape and provide strategic insights to clients.
2. How have you supported regulatory professional services or projects in your previous role? Answer: In my previous role, I actively supported regulatory professional services and projects. I collaborated with cross-functional teams to ensure the successful delivery of projects within the defined timelines and budget. I assisted in project coordination, tracking, and addressing any risks or delivery issues that arose. I also contributed to the development of customer-facing materials and provided regulatory intelligence support to clients. This experience has honed my ability to manage projects and provide effective regulatory solutions.
3. Can you describe your experience in handling customer-facing interactions or providing customer service in a regulatory context? Answer: Throughout my career, I have had direct customer-facing interactions and provided customer service in the field of regulatory affairs. I have effectively communicated with clients, understood their requirements, and provided them with regulatory guidance and solutions. I am skilled in building strong client relationships, addressing their queries, and ensuring their satisfaction with the services provided. This experience has enhanced my ability to understand customer needs and deliver value-added regulatory consulting services.
4. How do you approach problem management, troubleshooting, and analysis within the regulatory domain? Answer: I approach problem management, troubleshooting, and analysis in a systematic and analytical manner. When faced with challenges, I thoroughly analyze the situation, identify the root cause, and propose appropriate solutions. I have a strong attention to detail and a proactive approach to problem-solving. Additionally, I leverage my knowledge of regulatory guidelines and industry best practices to navigate complex issues and provide effective resolutions. This approach has helped me successfully manage regulatory projects and ensure compliance.
5. Can you provide examples of your experience working with virtual teams and successfully delivering projects? Answer: In my previous role, I worked extensively with virtual teams and successfully delivered projects in a collaborative environment. I effectively communicated and coordinated with team members located in different regions and time zones. I utilized project management tools and technologies to facilitate seamless collaboration and track project progress. By fostering open communication, setting clear expectations, and leveraging each team member’s expertise, we achieved project milestones and delivered high-quality outcomes. This experience has strengthened my ability to work in diverse teams and manage projects efficiently.

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