Regulatory Affairs/Pharmacovigilance Project Manager

თარიღები: 07 ოქტ - 05 ნოემ
მდებარეობა: თბილისი
დასაქმების ფორმა: სრული განაკვეთი
განათლება: ბაკალავრი
ენები: ინგლისური

სხვა ვებ გვერდზე

სხვა:  პროექტის მართვა

Regulatory Affairs/Pharmacovigilance Project Manager

Excellent opportunity for fresh graduates!

By joining our international team you will work closely with colleagues from different countries and departments and you will be a key contact person for our clients for new products and compliance-related issues. You will be able to work from home as a contractor, with a regular 8 hours a day schedule.

 

To be successful in this role you need to:

  • Be proficient in written and spoken English; knowledge of other languages is a distinctive advantage.
  • Understand project management principles.
  • Knowledge of Product Life Cycle Management and EU regulations and guidelines is an advantage Experience of eCTD would also be beneficial.
  • University degree or equivalent experience in Life Sciences (Chemistry, Pharmacology, Biology, Medicine, etc.) is an advantage.
  • Be flexible and adaptable to changing project priorities and work assignments
  • Be able to work under strict timelines
  • Have excellent communication skills

 

Your responsibilities will be:

 

General Project Management

  • Design and implement project plans by coordinating with other departments as well as with clients to ensure that projects are implemented, deadlines are met and deliverables are of high quality.
  • Identify and report project and deliverable related risks to direct managers or relevant experts.
  • Follow current Standard Operating Procedures (SOP) guidelines regarding procedural steps throughout the entire life cycle of the project.
  • Act as (Single) Point of Contact and oversee clients’ portfolios.

 

Regulatory Affairs

  • Submit registration and maintenance documents to regulatory agencies and carry out all the subsequent negotiations and activities necessary to obtain and maintain the marketing authorization for the products.
  • Work closely with government agencies to ensure all legislation is closely followed and the clients’ products comply with the regulations.

 

Pharmacovigilance

  • Function as interface for clients regarding project management activities including deliverables as per service agreement and technical agreement.
  • Liaise and coordinate with local responsible PV personnel/ local PV representatives in EU for ensuring local pharmacovigilance activities for the client.
  • Coordinate with QPPV and PV team for relevant safety/PV requests from client.
  • Coordinate with the client for specific data for PSURs, PSMF and RMP and other reports.
  • Ensure that local literature search and monitoring of local health authorities’ website is performed.
  • Assist in invoicing and billing related queries with finance and admin team.
  • Prepare monthly PV activity reports, review and communicate with different clients regarding ongoing quality and compliance PV activities.
  • Attend regular teleconferences with clients, technical team and experts to ensure smooth project flow.
  • Use project management database for clear project status and closure.

 

JOB CATEGORY: Project Management

JOB LOCATION: anywhere in the world

JOB TYPE: Full Time

 

CONTACT PERSON:

Andrea Szekely HR Generalist

+40 364 730 401

andrea.szekely@elc-group.com

 

It is also possible to send the CV via our web-site https://elc-group.com/jobs/regulatory-affairs-pharmacovigilance-project-manager

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