Medical Affairs Associate

min €36 EUR / hour

Kapalı

İlan edilme:

4 yıldan fazla önce

min €36 EUR / hour

As a Medical Affairs Associate, you will support the Qualified Person Responsible for Information and Publicity (QP RIP) in the review and approval of promotional activities and materials for multiple pharmaceutical companies in Benelux and contribute in pharmacovigilance projects. Promotional material & activities: - Advice the Marketing departments of several MAHs in developing strong but compliant promo materials - Review and approve promotional activities in compliance with legislation on advertising and promotion Obtain approval from Authorities for advertising to the general public, incl. TV or radio commercials - Install or improve local Healthcare Compliance SOPs - Upload or facilitate the preparation of the transparency file for [login to view URL] or transparantieregister Pharmacovigilance: - Local Literature Review for the MAHs medicinal products - Risk Minimisation Acvtivities: agree with authorities and distribute RMA material - PV quality system set-up or maintenance: PV SOP's, gap analysis, compliance checks - Act as (back-up) Local Contact Person for pharmacovigilance - Provide PV awareness training to MAHs employees Interested in the vacancy? Check out the entire vacancy in attachment.

Medical

Proje No: 23367569

Proje hakkında

11 teklif

Uzaktan proje

Son aktiviteden bu yana geçen zaman 4 yıl önce

Biraz para mı kazanmak istiyorsunuz?

E-posta adresi

Freelancer'da teklif vermenin faydaları

Bütçenizi ve zaman çerçevenizi belirleyin

Çalışmanız için ödeme alın

Teklifinizin ana hatlarını belirleyin

Kaydolmak ve işlere teklif vermek ücretsizdir

11 freelancers are bidding on average €37 EUR/ saat for this job

@drmansigurbani7

Hello, Greetings!! I am a certified Pharmocovigilance expert. (Clinical Research Professional) with a degree in Dentistry. I have worked as an Quality analyst and Quality check (Drug safety associate) on different projects handled by IQVIA. (where I worked for ROCHE and Pfizer). I am very much interested in working on this project. My bid is as per your stated budget, but we can discuss more on the same, if given chance. If vacancy persists, I will be glad to hear from you. (P.S: I want to let you know that somehow the attachement you have shared is not working. If possible please reshare the same.) Thank you, Kind regards, Dr. Mansi Dawesar.

€36 EUR 40 gün içinde

0,0

(0 değerlendirme)

0,0

@Sayk99

As i am a medical doctor and have experiance of working as managing director of a pharmaceutical company, it would be the best to assisst in this sector. Being in field i can deliver the best

€36 EUR 40 gün içinde

0,0

(0 değerlendirme)

0,0

@mayelalabarca

you'll get help from an internal medicine specialist t a non Invasive clinical research cardiologist with a Master in Cardiovascular Deseases, who fluently fluently speaks/reads/writes in English and Spanish and experience writing for medical journals like circulation. Please check my portfolio.

€36 EUR 30 gün içinde

0,0

(0 değerlendirme)

0,0

@shahzad695

I am an experienced medical professional (Pharmacist), additionally have an MBA marketing degree. For last 3 years I am working in a Govt Hospital, Previously I worked in a pharmaceutical company (GSK) for 5 years .

€36 EUR 40 gün içinde

0,0

(0 değerlendirme)

0,0

@bossmangidi1

Hopefully will be done within the next 5 days fast reliable sources always online seeking your new works .

€37 EUR 5 gün içinde

0,0

(0 değerlendirme)

0,0

@srinathvarma88

Hi, Warm Greetings! The roles and responsibilities specified in the above description is highly relevant to my accumulated experience and skills as a drug safety scientist in various contract research organizations and multinational companies, which stimulated me for this proposal. I would like to take this as an opportunity to disseminate my pharmacovigilance knowledge in multiple therapeutic areas to respective customer/MAH by contributing to various domains in PV. Below are my recent milestones included: As Functional Lead, established 3 local literature projects (2 European MAH and 1 Japan based MAH). Victorious completion of Dutch Health authority Inspection held at Netherlands office of MAH with no critical and major findings. I'm the Lead presenter for entire process and answering multiple questions from Inspector in the operations process on behalf of MAH. I would like to decipher my overall achievements when we had good time for a discussion. Please contact me, If you would like to liaise with me for further communications. Patient safety is first, Always compliant :) Many Thanks! Best Regards, Srinath

€36 EUR 40 gün içinde

0,0

(0 değerlendirme)

0,0

@khushboo624

I've around 07 years of experience in pharmacovigilance

€40 EUR 10 gün içinde

0,0

(0 değerlendirme)

0,0

@dreamtoucher1

Hi! I'm a practicing physician in general surgery. I have graduated medical school in Moscow, Russia and did my surgical residency there. Lived in Chicago, United States for 5 years, now live in Istanbul, Turkey. I'm native speaker in Russian. Also I'm fluent English speaker, writer and reader. Have an experience in teaching basic sciences such as biology, chemistry, physics as well as clinical subjects such as surgery and clinical pharmacology.

€36 EUR 80 gün içinde

0,0

(0 değerlendirme)

0,0

@jokergirl222

Hello All, My name is Mai Elshewikh, QA officer working in medical devices and pharmaceutical for about five yearsISO 13485,EMEA, GMP,CAPA cordinator,Internal Auditor.I am veterinarian live in Brussel

€36 EUR 10 gün içinde

0,0

(0 değerlendirme)

0,0

@rucks19

I have more than an year of experience as a medical Reviewer in Pharmacovigilance with working knowledge and experience in US FDA and EMA reporting GUIDELINES. Relevant Skills and Experience Worked ICSR,aggregate as well as Signal management processes.

€40 EUR 40 gün içinde