💼 Biomapas - Pharmacovigilance Assistant
✍🏻 As Pharmacovigilance Assistant, you will be assisting in the survey and monitoring of national pharmacovigilance regulations, ensuring successful communication with local Competent Authorities, assisting in the processes of proper collection, duplicate check, processing, accurate translation, quality control (at least second self-control), documentation, reporting and follow-up of all safety reports and similar.
Career level: Entry Level (Graduates)
📍 Kaunas/Vilnius #Lithuania
#Pharmacovigilance
ℹ️ http://bit.ly/2FEBvEK
✍🏻 As Pharmacovigilance Assistant, you will be assisting in the survey and monitoring of national pharmacovigilance regulations, ensuring successful communication with local Competent Authorities, assisting in the processes of proper collection, duplicate check, processing, accurate translation, quality control (at least second self-control), documentation, reporting and follow-up of all safety reports and similar.
Career level: Entry Level (Graduates)
📍 Kaunas/Vilnius #Lithuania
#Pharmacovigilance
ℹ️ http://bit.ly/2FEBvEK
💼 BIAL - Regional Marketing Assistant
✍🏻 You will be responsible for supporting and executing marketing strategies for BIAL’s products within the different geographical areas represented in the Emerging Markets. Specifically, you will support the development and manage the approvals of the brand kit deliverables (training manual, scientific promotional material development and adjustment to different markets, material for congresses and presentations, printing add, etc.).
Languages: French or Spanish (fluent)
Career level: Entry Level (Graduates) and Junior
📍 Porto #Portugal
#SalesAndMarketing
ℹ️ http://bit.ly/2YxzfX9
✍🏻 You will be responsible for supporting and executing marketing strategies for BIAL’s products within the different geographical areas represented in the Emerging Markets. Specifically, you will support the development and manage the approvals of the brand kit deliverables (training manual, scientific promotional material development and adjustment to different markets, material for congresses and presentations, printing add, etc.).
Languages: French or Spanish (fluent)
Career level: Entry Level (Graduates) and Junior
📍 Porto #Portugal
#SalesAndMarketing
ℹ️ http://bit.ly/2YxzfX9
💼 Merck - Internship Global Market Access and Pricing
✍🏻 You will play a key role in operational pricing, i.e. you will analyze price change requests - considering short- and long-term impact across regions –, help the countries to find the optimal price and drive alignment within regional and global stakeholders. You will also be asked to prepare price reports for internal and/or external use.
On top of pricing related topics, you will also support the development of payer-targeted value communication tools, which aim to support our local teams to communicate the value of the respective product to payers appropriately. You will be, during your internship, an integral part of the global pricing and market access team. You will, after an introduction period, interact directly with the various national market leaders of market access and pricing and senior leaders at the regional and global level.
Career level: Entry level (Students)
📍 Darmstadt #Germany
#MarketAccess
ℹ️ http://bit.ly/2UeC5RN
📆 Originally posted: 16/03/2019
✍🏻 You will play a key role in operational pricing, i.e. you will analyze price change requests - considering short- and long-term impact across regions –, help the countries to find the optimal price and drive alignment within regional and global stakeholders. You will also be asked to prepare price reports for internal and/or external use.
On top of pricing related topics, you will also support the development of payer-targeted value communication tools, which aim to support our local teams to communicate the value of the respective product to payers appropriately. You will be, during your internship, an integral part of the global pricing and market access team. You will, after an introduction period, interact directly with the various national market leaders of market access and pricing and senior leaders at the regional and global level.
Career level: Entry level (Students)
📍 Darmstadt #Germany
#MarketAccess
ℹ️ http://bit.ly/2UeC5RN
📆 Originally posted: 16/03/2019
💼 Merck - Internship Scientific Support Global Medical Affairs Fertility
✍🏻 You will be involved in international projects for Merck's most important brands from a medical and scientific perspective e.g. new therapeutic strategies, real world data analyses, clinical trials or launch of the products in new markets. Amongst other tasks this will include literature searches, analysis of data, creation of scientific presentations and support in the preparation of major international meetings (i.e. ESHRE) and Ad Boards.
Career level: Entry Level (Students and Graduates)
📍 Darmstadt #Germany
#MedicalAffairs
ℹ️ http://bit.ly/2U72BwR
📆 Originally posted: 23/03/2019
✍🏻 You will be involved in international projects for Merck's most important brands from a medical and scientific perspective e.g. new therapeutic strategies, real world data analyses, clinical trials or launch of the products in new markets. Amongst other tasks this will include literature searches, analysis of data, creation of scientific presentations and support in the preparation of major international meetings (i.e. ESHRE) and Ad Boards.
Career level: Entry Level (Students and Graduates)
📍 Darmstadt #Germany
#MedicalAffairs
ℹ️ http://bit.ly/2U72BwR
📆 Originally posted: 23/03/2019
💼 CSL - EU Regulatory Affairs Scientist
✍🏻 The Regulatory Affairs Scientist EU is responsible for regional regulatory strategic and operational tasks for products licensed in the EU market or under clinical development within the Immunology and Neurology Therapeutic Area.
Career level: Entry Level (Graduates) and Junior
📍 Bern #Switzerland or Marburg #Germany
#RegulatoryAffairs
ℹ️ http://bit.ly/2ODHqwF
📆 Originally posted: 27/03/2019
✍🏻 The Regulatory Affairs Scientist EU is responsible for regional regulatory strategic and operational tasks for products licensed in the EU market or under clinical development within the Immunology and Neurology Therapeutic Area.
Career level: Entry Level (Graduates) and Junior
📍 Bern #Switzerland or Marburg #Germany
#RegulatoryAffairs
ℹ️ http://bit.ly/2ODHqwF
📆 Originally posted: 27/03/2019
💼 GSK - Future Leaders Programme - Supply Chain
✍🏻 Over three years, the Future Leaders graduate programme will challenge and support you to grow professionally and personally. You’ll have three stretching rotations within pharmaceutical or consumer healthcare supply, depending on your area. In both cases, you’ll take on business-critical roles that offer insights into end-to-end supply chain. You’ll learn about the synergies and challenges that come with delivering optimum value to the business and the customer.
Languages: French (basic)
❗️ Deadline: 19/05/2019
Career level: Entry level (Graduates)
📍 Nyon #Switzerland
#SupplyChain
ℹ️ http://bit.ly/2YLVA3h
✍🏻 Over three years, the Future Leaders graduate programme will challenge and support you to grow professionally and personally. You’ll have three stretching rotations within pharmaceutical or consumer healthcare supply, depending on your area. In both cases, you’ll take on business-critical roles that offer insights into end-to-end supply chain. You’ll learn about the synergies and challenges that come with delivering optimum value to the business and the customer.
Languages: French (basic)
❗️ Deadline: 19/05/2019
Career level: Entry level (Graduates)
📍 Nyon #Switzerland
#SupplyChain
ℹ️ http://bit.ly/2YLVA3h
💼 GSK - Future Leaders Programme - Manufacturing Operations
✍🏻 Over two years, the Future Leaders graduate programme will challenge and support you to grow professionally and personally. You’ll have three stretching rotations that will give you an insightful experience into the manufacturing side of the vaccines business. You start with a one-year rotation on the shop floor at the centre of the technical functions (e.g. Maintenance and Engineering). This will be followed by a six-month rotation in Quality and a further six months in Supply Chain Management. One of the two six months rotations will be based abroad. Through these placements, you’ll develop your expertise in Technical Services, Quality and Supply Chain Management, while broadening your global business perspective.
Languages: German (fluent)
❗️ Deadline: 29/05/2019
Career level: Entry level (Graduates)
📍 Dresden #Germany
#Production #Quality #SupplyChain
ℹ️ http://bit.ly/2COC9xs
✍🏻 Over two years, the Future Leaders graduate programme will challenge and support you to grow professionally and personally. You’ll have three stretching rotations that will give you an insightful experience into the manufacturing side of the vaccines business. You start with a one-year rotation on the shop floor at the centre of the technical functions (e.g. Maintenance and Engineering). This will be followed by a six-month rotation in Quality and a further six months in Supply Chain Management. One of the two six months rotations will be based abroad. Through these placements, you’ll develop your expertise in Technical Services, Quality and Supply Chain Management, while broadening your global business perspective.
Languages: German (fluent)
❗️ Deadline: 29/05/2019
Career level: Entry level (Graduates)
📍 Dresden #Germany
#Production #Quality #SupplyChain
ℹ️ http://bit.ly/2COC9xs
💼 Bayer - Pharmaceutical Production & Quality Trainee/Graduate - International Future Leadership Program
✍🏻 The 24-month International Future Leadership Trainee/Graduate Program aims at introducing you to and preparing you for a management position within Bayer’s global Production and Quality functions with a wide range of challenging, cross-divisional and cross-functional roles and responsibilities as well as a strong, supportive global network.
You will specifically focus on and contribute towards gaining a broad overview on key pharmaceutical manufacturing units regarding technological, operational, quality-related good manufacturing practices and leadership aspects, understanding the pharmaceutical supply chain and the global manufacturing network and taking over and conclude operational tasks and projects to build up practical experience.
❗️ Deadline: 14/04/2019
Career level: Entry Level (Graduates)
📍 Berlin #Germany
#Production #Quality
ℹ️ http://bit.ly/2TRlFu5
✍🏻 The 24-month International Future Leadership Trainee/Graduate Program aims at introducing you to and preparing you for a management position within Bayer’s global Production and Quality functions with a wide range of challenging, cross-divisional and cross-functional roles and responsibilities as well as a strong, supportive global network.
You will specifically focus on and contribute towards gaining a broad overview on key pharmaceutical manufacturing units regarding technological, operational, quality-related good manufacturing practices and leadership aspects, understanding the pharmaceutical supply chain and the global manufacturing network and taking over and conclude operational tasks and projects to build up practical experience.
❗️ Deadline: 14/04/2019
Career level: Entry Level (Graduates)
📍 Berlin #Germany
#Production #Quality
ℹ️ http://bit.ly/2TRlFu5
💼 Roche - (Junior) Quality Assurance Manager
✍🏻 As a (Junior) Quality Assurance Manager within QA Finished Goods (Sterile Packaging), you are responsible for the supervision of all release-relevant processes of sterile finished medicinal products. In this function, you ensure that the legal requirements, the GMP and the Roche guidelines are adhered to and support the packaging companies and interface areas (e.g. logistics, quality control, packaging development) in all aspects of GMP compliance.
Languages: German (fluent)
Career level: Entry Level (Graduates) and Junior
📍 Kaiseraugst #Switzerland
#Quality
ℹ️ http://bit.ly/2VozoKG
📆 Originally posted: 02/04/2019
✍🏻 As a (Junior) Quality Assurance Manager within QA Finished Goods (Sterile Packaging), you are responsible for the supervision of all release-relevant processes of sterile finished medicinal products. In this function, you ensure that the legal requirements, the GMP and the Roche guidelines are adhered to and support the packaging companies and interface areas (e.g. logistics, quality control, packaging development) in all aspects of GMP compliance.
Languages: German (fluent)
Career level: Entry Level (Graduates) and Junior
📍 Kaiseraugst #Switzerland
#Quality
ℹ️ http://bit.ly/2VozoKG
📆 Originally posted: 02/04/2019
💼 Roche - Student Internship Evidence and Policy
✍🏻 You will help to develop a new evidence dossier template and global health policy plan for Roche Diabetes Care (RDC) as well as a knowledge management platform. These projects will support RDC affiliates globally to address evidence needs around newly developed products and solutions. You will work develop and administer surveys, which seek to identify the evidence needs from affiliate countries, while at the same time to layout the current health policy landscape. The survey results will inform the design of the evidence dossier template. You will also be responsible for assessing and documenting regional activities (e.g. participation in policy or advisory organisations) for Roche Diabetes Care.
Career level: Entry level (Students)
📍 Basel #Switzerland
#Policy
ℹ️ http://bit.ly/2IdWM9V
📆 Originally posted: 03/04/2019
✍🏻 You will help to develop a new evidence dossier template and global health policy plan for Roche Diabetes Care (RDC) as well as a knowledge management platform. These projects will support RDC affiliates globally to address evidence needs around newly developed products and solutions. You will work develop and administer surveys, which seek to identify the evidence needs from affiliate countries, while at the same time to layout the current health policy landscape. The survey results will inform the design of the evidence dossier template. You will also be responsible for assessing and documenting regional activities (e.g. participation in policy or advisory organisations) for Roche Diabetes Care.
Career level: Entry level (Students)
📍 Basel #Switzerland
#Policy
ℹ️ http://bit.ly/2IdWM9V
📆 Originally posted: 03/04/2019
💼 AstraZeneca - Summer Internship Programme
✍🏻 You will undergo role-specific training and you will be mentored by highly experienced professionals. You will have the opportunity to learn about AstraZeneca and a global pharmaceutical company work environment, as well as learn about different departments, from both global and local level. You will be able to experience various areas in R&D (Study Management & Operations, Site Management & Monitoring, Processes & Enabling Solutions, Clinical Trial Safety, Regulatory Project Management) and/or Commercial (Commercial Excellence, Finance, Procurement).
You will undertake real work, proactively collaborating with experienced staff. At the end of your internship you will receive a certificate and a detailed feedback from the programme team.
❗️ Deadline: 30/05/2019
Career level: Entry Level (Students and Graduates)
📍 Warsaw #Poland
#Various
ℹ️ http://bit.ly/2uPAQtM
📆 Originally posted: 05/04/2019
✍🏻 You will undergo role-specific training and you will be mentored by highly experienced professionals. You will have the opportunity to learn about AstraZeneca and a global pharmaceutical company work environment, as well as learn about different departments, from both global and local level. You will be able to experience various areas in R&D (Study Management & Operations, Site Management & Monitoring, Processes & Enabling Solutions, Clinical Trial Safety, Regulatory Project Management) and/or Commercial (Commercial Excellence, Finance, Procurement).
You will undertake real work, proactively collaborating with experienced staff. At the end of your internship you will receive a certificate and a detailed feedback from the programme team.
❗️ Deadline: 30/05/2019
Career level: Entry Level (Students and Graduates)
📍 Warsaw #Poland
#Various
ℹ️ http://bit.ly/2uPAQtM
📆 Originally posted: 05/04/2019
💼 Novo Nordisk - Safety Medical Writer
✍🏻 As a Safety Medical Writer in Safety Surveillance Reporting, you will be responsible for planning and managing document preparation (Development Safety Update Reports [DSURs], Periodic Safety Update Reports [PSURs], and Clinical Risk Management Plans [RMPs]) and responses to Health Authority questions in a cross-functional environment and ensuring high quality scientific writing.
You will work in close collaboration with Safety Surveillance Advisors, Medical Specialists from Global Development, Medical Advisors from Medical Affairs, Project Managers from Regulatory Affairs, and Safety Publishers. While your key responsibilities will include preparing the key safety reporting documents you will also be expected to actively contribute to process improvements and other projects.
❗️ Deadline: 29/04/2019
Career level: Entry Level (Graduates) and Junior
📍 Bagsværd #Denmark
#Pharmacovigilance
ℹ️ http://bit.ly/2ULkbpR
✍🏻 As a Safety Medical Writer in Safety Surveillance Reporting, you will be responsible for planning and managing document preparation (Development Safety Update Reports [DSURs], Periodic Safety Update Reports [PSURs], and Clinical Risk Management Plans [RMPs]) and responses to Health Authority questions in a cross-functional environment and ensuring high quality scientific writing.
You will work in close collaboration with Safety Surveillance Advisors, Medical Specialists from Global Development, Medical Advisors from Medical Affairs, Project Managers from Regulatory Affairs, and Safety Publishers. While your key responsibilities will include preparing the key safety reporting documents you will also be expected to actively contribute to process improvements and other projects.
❗️ Deadline: 29/04/2019
Career level: Entry Level (Graduates) and Junior
📍 Bagsværd #Denmark
#Pharmacovigilance
ℹ️ http://bit.ly/2ULkbpR
💼 Novo Nordisk - Regulatory Professional in Regulatory Operations
✍🏻 As a Regulatory Professional, you will coordinate the activities around the RIM system and processes and provide expert process guidance to relevant stakeholders across the organisation. The RIM system contains information about all marketed products and devices at the company and in close collaboration with stakeholders from the Regulatory Products Groups and Therapeutic Areas you will ensure that data is correct, up to date and available in the system at all times.The RIM system and process support order generation, batch allocation and correct batch releases. Therefore, you will also be central point of contact for many stakeholders outside Regulatory Affairs such as Product Supply, Quality and Logistics globally, whom you will be collaborating with to support that the right product variants reach the market and thereby the patients.
You will also drive optimisation activities and participate in major process transformation projects. Together with stakeholders, you will therefore work on identifying simple solutions that both comply with (new) regulatory requirements and ensure best in class processes.
❗️ Deadline: 22/04/2019
Career level: Junior
📍 Søborg #Denmark
#Regulatory Operations
ℹ️ http://bit.ly/2KkSMY0
✍🏻 As a Regulatory Professional, you will coordinate the activities around the RIM system and processes and provide expert process guidance to relevant stakeholders across the organisation. The RIM system contains information about all marketed products and devices at the company and in close collaboration with stakeholders from the Regulatory Products Groups and Therapeutic Areas you will ensure that data is correct, up to date and available in the system at all times.The RIM system and process support order generation, batch allocation and correct batch releases. Therefore, you will also be central point of contact for many stakeholders outside Regulatory Affairs such as Product Supply, Quality and Logistics globally, whom you will be collaborating with to support that the right product variants reach the market and thereby the patients.
You will also drive optimisation activities and participate in major process transformation projects. Together with stakeholders, you will therefore work on identifying simple solutions that both comply with (new) regulatory requirements and ensure best in class processes.
❗️ Deadline: 22/04/2019
Career level: Junior
📍 Søborg #Denmark
#Regulatory Operations
ℹ️ http://bit.ly/2KkSMY0
💼 Roche - Student Internship in Technical Regulatory Affairs
✍🏻 As an Intern, you will gain insight into the work of Technical Regulatory Affairs professionals who are responsible for providing the regulatory input and leadership for quality-related aspects of pharmaceuticals. The activities span the whole lifecycle of the product, from clinical trials all the way to the maintenance of products at the end of their lifecycle.
Career level: Entry level (Students)
📍 Basel #Switzerland
#RegulatoryAffairs
ℹ️ http://bit.ly/2Uxg3ux
✍🏻 As an Intern, you will gain insight into the work of Technical Regulatory Affairs professionals who are responsible for providing the regulatory input and leadership for quality-related aspects of pharmaceuticals. The activities span the whole lifecycle of the product, from clinical trials all the way to the maintenance of products at the end of their lifecycle.
Career level: Entry level (Students)
📍 Basel #Switzerland
#RegulatoryAffairs
ℹ️ http://bit.ly/2Uxg3ux
💼 AstraZeneca - Associate Scientist – Analytical Sciences
✍🏻 You will play an important role in early drug development programmes by supporting the analytical characterisation of novel proteins (from peptides to antibodies) through method development, method qualification, batch release and stability assessment. You will also participate in the development of new analytical techniques within the Analytical Sciences team as well as perform analytical testing (using a variety of techniques) to assess the quality of AstraZeneca products for use in formulation, pharmacology and all other applications.
Career level: Entry Level (Graduates) and Junior
📍 Cambridge #UK
#ResearchAndDevelopment
ℹ️ http://bit.ly/2X2HzMW
📆 Originally posted: 05/04/2019
✍🏻 You will play an important role in early drug development programmes by supporting the analytical characterisation of novel proteins (from peptides to antibodies) through method development, method qualification, batch release and stability assessment. You will also participate in the development of new analytical techniques within the Analytical Sciences team as well as perform analytical testing (using a variety of techniques) to assess the quality of AstraZeneca products for use in formulation, pharmacology and all other applications.
Career level: Entry Level (Graduates) and Junior
📍 Cambridge #UK
#ResearchAndDevelopment
ℹ️ http://bit.ly/2X2HzMW
📆 Originally posted: 05/04/2019
💼 Novartis - Regulatory Affairs Postgraduate Training Program
✍🏻 The Regulatory Affairs Postgraduate Training Program is an opportunity to discover the global functions of Regulatory Affairs and Regulatory Chemistry, Manufacturing and Controls.
Successful candidates will be offered a training position consisting of two rotational assignments, each of 1 year duration, within two different RA functions.
❗️ Deadline: 31/05/2019
Career level: Entry Level (Graduates)
📍 Basel #Switzerland
#RegulatoryAffairs
ℹ️ http://bit.ly/2XaOBj3
✍🏻 The Regulatory Affairs Postgraduate Training Program is an opportunity to discover the global functions of Regulatory Affairs and Regulatory Chemistry, Manufacturing and Controls.
Successful candidates will be offered a training position consisting of two rotational assignments, each of 1 year duration, within two different RA functions.
❗️ Deadline: 31/05/2019
Career level: Entry Level (Graduates)
📍 Basel #Switzerland
#RegulatoryAffairs
ℹ️ http://bit.ly/2XaOBj3
💼 Novo Nordisk - Associate Scientist for Formulation & Delivery
✍🏻 As an Associate Scientist in Formulation & Delivery your main objective will be to decide and secure formulations and analyses for in vivo studies of primarily peptides and proteins, but also other molecular formats. You will be part of interdisciplinary project teams comprising diverse competencies spanning across multiple natural sciences and engineering disciplines in our R&D organisation.
Your main task will be to contribute with your knowledge of molecular characteristics, formulation and biophysics in combination with an understanding of in vivo studies and animal welfare. Based on your knowledge you will design and conduct experiments to support research and drug development. This job will offer you a high level of independence and flexibility within the research project framework and you will work closely together with other departments in Denmark or research sites outside Denmark.
❗️ Deadline: 27/03/2019
Career level: Entry Level (Graduates) and Junior
📍 Måløv #Denmark
#ResearchAndDevelopment
ℹ️ http://bit.ly/2X5fViy
✍🏻 As an Associate Scientist in Formulation & Delivery your main objective will be to decide and secure formulations and analyses for in vivo studies of primarily peptides and proteins, but also other molecular formats. You will be part of interdisciplinary project teams comprising diverse competencies spanning across multiple natural sciences and engineering disciplines in our R&D organisation.
Your main task will be to contribute with your knowledge of molecular characteristics, formulation and biophysics in combination with an understanding of in vivo studies and animal welfare. Based on your knowledge you will design and conduct experiments to support research and drug development. This job will offer you a high level of independence and flexibility within the research project framework and you will work closely together with other departments in Denmark or research sites outside Denmark.
❗️ Deadline: 27/03/2019
Career level: Entry Level (Graduates) and Junior
📍 Måløv #Denmark
#ResearchAndDevelopment
ℹ️ http://bit.ly/2X5fViy
💼 Novo Nordisk - Clinical Research Associate, Clinical Development Center
✍🏻 The Clinical Research Associate (CRA) acts as site manager between site staff and Novo Nordisk, working within Polish Affiliate supporting one or more clinical trial(s) in a development programme. CRA is responsible for trial deliverables and ensuring the highest possible data quality in Novo Nordisk clinical trial(s).
The position is based in Warsaw, reports to Clinical Team Leader, Poland and will require travelling up to 60% of the time.
Languages: Polish (Fluent)
Career level: Junior
📍 Warsaw #Poland
#Clinical
ℹ️ http://bit.ly/2J8WRO3
✍🏻 The Clinical Research Associate (CRA) acts as site manager between site staff and Novo Nordisk, working within Polish Affiliate supporting one or more clinical trial(s) in a development programme. CRA is responsible for trial deliverables and ensuring the highest possible data quality in Novo Nordisk clinical trial(s).
The position is based in Warsaw, reports to Clinical Team Leader, Poland and will require travelling up to 60% of the time.
Languages: Polish (Fluent)
Career level: Junior
📍 Warsaw #Poland
#Clinical
ℹ️ http://bit.ly/2J8WRO3
🎧 The seventh episode of the Pharmadelic Experience podcast on From Academia to the Diverse World of Consulting with Andrei Baiceanu is now live!
In this episode we continue exploring unconventional career paths, this time Consulting.
We talked about Andrei's switch from Academia to Consulting in R&D and Regulatory Affairs, as well as what consulting is all about. He shared interesting insights about the recent project he worked on in top 20 pharma company. As usual, the podcast is packed with practical career advice!
I hope it inspires you as much as it inspired us and we hope you will be brave enough to try something different!
You can listen to the podcast on your favourite platform:
🔸 SoundCloud: http://bit.ly/2V2qK7B
🔸 Anchor: http://bit.ly/2Z4UWhw
🔸 iTunes: https://apple.co/2CzIttj
🔸 Spotify: https://spoti.fi/2pU9Yq5
💭 Do you have any comments, feedback or an interesting career story to share? Send us an email to feedback@pharmadelic.com or message us directly on Facebook or Instagram @Pharmadelic!
#PharmadelicExperience
In this episode we continue exploring unconventional career paths, this time Consulting.
We talked about Andrei's switch from Academia to Consulting in R&D and Regulatory Affairs, as well as what consulting is all about. He shared interesting insights about the recent project he worked on in top 20 pharma company. As usual, the podcast is packed with practical career advice!
I hope it inspires you as much as it inspired us and we hope you will be brave enough to try something different!
You can listen to the podcast on your favourite platform:
🔸 SoundCloud: http://bit.ly/2V2qK7B
🔸 Anchor: http://bit.ly/2Z4UWhw
🔸 iTunes: https://apple.co/2CzIttj
🔸 Spotify: https://spoti.fi/2pU9Yq5
💭 Do you have any comments, feedback or an interesting career story to share? Send us an email to feedback@pharmadelic.com or message us directly on Facebook or Instagram @Pharmadelic!
#PharmadelicExperience
Pharmadelic pinned «🎧 The seventh episode of the Pharmadelic Experience podcast on From Academia to the Diverse World of Consulting with Andrei Baiceanu is now live! In this episode we continue exploring unconventional career paths, this time Consulting. We talked about Andrei's…»