LIMS CLINICAL RESEARCH ANALYST BANGALORE

Posted 21 Dec 2021

Bangalore, Karnataka - India

Req Id 236235

Details

 

A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.

 

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 


 

BANGALORE hiring LIMS Clinical research professionals

 

 

We are hiring for LIMS CLINICAL RESEARCH ANALYST BANGALORE having 3 to 7 years work experience relevant to LIMS, CLINICAL OPERATION, CLINICAL STUDIES, ICF and eTMF domain.

Role: an exciting opportunity has arisen to join our healthcare business to support the development of first and outstanding specialty medicines for our patients in need. Resource will work in a new established group, that provides support for study teams of Phase I - Phase IV (interventional & non-interventional) and Investigator Sponsored Studies. Resource will run activities within a dedicated Center of Excellence for operational results of Clinical Studies with interactions of multiple cross functional Biopharma functions and CROs.

 

Job Responsibilities:

  • Resource will provide support to the Biosample Operation Leads and the Bioanalytical Operation Managers responsible for the operational implementation and execution of the translational medicine strategy in assigned clinical trials. Also will run set up and maintenance of studies in the Biosample Information database in collaboration with Operation Lead assigned to the clinical study.
  • Talent will also support operation activities by proof reading site training materials and handling instructions in regard to Biomarker/Biosample operational aspects.
  • Will also review sample inventories and reports provided by central laboratory, perform quality checks on patient consent attribute log files, Maintains oversight of sample reconciliation against consent (ICFs) and electronic case report form data by checking report received from clinical CRO.

 

Resource will check clinical biomarker and PK/ADA relevant documentation(s) are filed in electronic Trial Master File. Will assist the BOL and Bioanalytical Operation Manager in preparation of audits and inspections, retrieve documents from CRO. Will look BAOM in leading invoice processing & tracking (incl. Purchase Order, Payment Tracking & Reporting) for bioanalytical vendors.

 

Person will handle Document Management System (ELDORADO) Uploads & approval flows for bioanalytical reports, supervise bioanalytical lab performance (Key Performance Indicators, timelines), support production of critical reagents, prioritize shipment to CRO and maintain inventory.

 

Also will support study closure activities related to Biosample disposal / relocation to bio-repository.

We will give platform to talent to maintain and continually update knowledge of applicable Policies, Quality Documents, conventions, tools, templates, instructions, Good Clinical Practice (ICH-GCP), applicable national regulation and ensures implementation for the conduct of the tasks.

 

Criteria:

Graduate or Post Graduate in Pharmacy or Life-Science with 3 to 7 years work experience in relevant to CLINICAL OPERATION, eTMF, LIMS, CLINICAL STUDIES and ICF domain

We will look for resource should have excellent command of English language (verbally and in writing), working in international/ multicultural cross functional matrix environment, good understanding of the policies and procedures of Clinical Operations and of ICH-GCP. Scope of attention to details, analytical & problem solver will be there. Resource will need to have good time and priority management, ability to work efficiently.

 

Strong digital literacy including knowledge of MS Office™ (Excel™, Word™, PowerPoint™), Outlook and Teams.

 

Experience with Lab Management Systems is of advantage

 

Why with us?

 

As an organization for us a good job is not just about money. In addition to competitive compensation and bonuses acknowledging excellent work, we also offer a wide range of benefits to everyone works for us.

360-degree feedback has been used since its rollout by approximately 24,700 employees, in 2019, more than 11.200 employees took part in our classroom training courses worldwide & At the end of 2019, women occupied 33% of leadership roles Group-wide.

 

A job at our organization also provides you with flexibility to adapt to your priorities in life and the security of a company that is already successful for more than 350 years.

We support a diverse workforce and are meaningful to your needs, regardless of location, cultural or ethnic background, family status or age. We want to make your life easier and your work even more exciting. We support personal and professional development of our employees in line with their strengths, ambitions and proficiencies, thereby laying the groundwork for an enriching and exciting career with our company.


 

What we offer:  With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

 

Curious? Apply and find more information at https://jobs.vibrantm.com

 

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