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HISTORY For 40 years, we have been passionate about what we do: drug development. Our story began in 1979 when Dr Rolland-Yves Mauvernay, convinced that many useful therapeutic products were abandoned before reaching their full potential, decided to found the Swiss-based Debiopharm Group. Having started with only two people, Debiopharm is now a group of five companies active in the life science areas of drug development, GMP manufacturing of proprietary drugs, diagnostic tools and investment management. Together with his son Thierry Mauvernay, they have built a team of well over 420 dedicated professionals. The Group is now headed up by Mr Thierry Mauvernay, driven by the same passion as his father. He is fully committed to the group’s current activities and planning the future to ensure long-term continuity. BUSINESS What we do We are a pharmaceutical research, development and production facility, inspected and registered with the main regulatory authorities. BUSINESS MODEL The Company is a world leader in polylactic-co-glycolic acid (PLGA)-based injectable, sustained-release technology. It has been used for one of our best-selling product Decapeptyl®, a novel injectable controlled-release formulation of triptorelin – a gonadotropin releasing hormone (GnRH) agonist analogue. This mode of administration developed by Debiopharm Research & Manufacturing relies on the active substance being “encapsulated” in a PLGA polymer to allow gradual dissolution and distribution of the substance in the patient’s body. The Company has succeeded in producing 1-month, 3-month and 6-month sustained-release (SR) formulations. It is also focusing on nanoparticular drug delivery systems. SOCIAL RESPONSIBILITY We are dedicated to contributing positively to the development and wellbeing of projects we believe in. We support various initiatives led by personalities who are true innovators or inspirers, as well as various philanthropic activities aiming at improving people and patient’s life.
Project ID: 19481445
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Active 7 yrs ago
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22 freelancers are bidding on average $19 USD/hour for this job

TO WHOM IT MAY CONCERN Please find enclosed my CV in application for the post published vacancy. The nature of my degree course has prepared me for this position. It involved great deal of independent research, requiring initiative, self- motivation and a wide range of skills. I am a conscientious person who works hard and pays attention to details. In addition, quick to pick up new skills and eager to learn from others and implement new techniques. I also have lots of ideas and enthusiasm and determination to ensure that I make success of it. I posses qualitative references and would be delighted to discuss any possible vacancy with you at your convenience. In case you do not have any suitable openings at the moment, I would be grateful if you would keep my CV on file for any possibilities. Thank you for taking the time to consider this application and I look forward hearing from you in the near future. Yours sincerely, MD,MSci M P
$22 USD in 40 days
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I am a software engineer I have more than six years in project management So I have the competence, experience and time to get the job done....
$17 USD in 40 days
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Hello, I am joe My transcripts accuracy ranges from 97-100% and as such proofreading is also what I can do perfectly for you. Expecting to hear from you. Thank you. Sincerely, Joe Relevant Skills and Experience I am a professional transcriber My transcripts accuracy ranges from 97-100% and as such proofreading is also what I can do perfectly for you
$22 USD in 10 days
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I am good at Copy Typing and Data Entry with some handful of experience offline. If given a chance, will prove my ability by delivering the work in time effectively.
$16 USD in 25 days
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I am an experienced data entry clerk who is available to do all data entry work. I have immense knowledge of Microsoft Word and Microsoft Excel. This makes me the best pick for this job. All the best with your business and I look forward to working with you!
$16 USD in 5 days
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Fresher and completed MBA Relevant Skills and Experience Typing and communication skills
$22 USD in 10 days
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I am currently in the transcription field and can handle what needs to be done in a timely manner. I currently have no time constraints and can get the work done. I have graduated with honors from University and have been doing my best to get a foothold in the freelance scene. I believe I can do great work for you all. Trust in me and I will give you everything.
$16 USD in 40 days
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Hi, my name is Allan Duron, from Honduras. I would love to work with you as a Data entry. I have over 9 years of experience in assisting management positions. I am completely proficient in the use of email, and online communication. I have great interpersonal relationships abilities. I can perfectly use Google Docs, Dropbox and Canva and I have advanced knowledge of Excel. I have experience taking care of some design work in Photoshop. I also have experience designing posts for Instagram, and FB events banner using Canva. I am completely bilingual, I have an IELTS certification on my English proficiency. I can work full time or part-time. Looking forward to hearing from you soon. Feel free to contact me directly if you have further questions.
$16 USD in 40 days
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Hello Sir, I am Jonardon Roy, study at SEGi University in Bachelor of Information Technology. I have confident that i can do your project appropriately. I hope you will give me the opportunity to work with you. Thank You.
$16 USD in 40 days
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Excellent project-management skills, great eye for details, all of which should make me an ideal candidate for this opening
$22 USD in 40 days
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I am very passionate about what i do whether it is my work, my gameplay(basketball) or my emotions towards someone. I am hard working, much focused and sustained to my work whatever given to me. Relevant Skills and Experience I can create excel sheet with all expertise. I have been doing thus since last 3-4 years for my family business as a helping hand.
$22 USD in 10 days
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I am a very methodical and detail oriented person with high time availability. I would be delighted to contribute with your company and I am looking forwards to knowing a little bit more about the job. Greetings Carolina
$16 USD in 45 days
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Hi, I am interested about your project. I am 6 year experienced data entry operator. I have proficient knowledge in excel ,word and access. You have fascinating company history. I like to join if you're interested in me. Thanks for your time
$16 USD in 40 days
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I am sayad basha done bachelor of pharmacy. I have 3 years experience in pharmaceutical company as a business development executive. Present I am not working so I am ready to work in your organization Relevant Skills and Experience I have relevant skills but I didn't have experience if u give me the opportunity I will work hard for better outcome. I am published some articles in journals
$18 USD in 40 days
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I'm excited for this job since I have ample experience in data entry and research. I am currently employed as Email Support and what I do is answer customers' queries thru e-mail. Hire me. Relevant Skills and Experience I have worked as an Abstractor for a publishing company. I read books and write abstracts so readers can get a glimpse of what they're buying. I'm comfortable with data processing and market research.
$22 USD in 10 days
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Good at typing fast and having knowledge of data entry also web search experience sir thank you Relevant Skills and Experience Data entry skills and copy paste skills
$15 USD in 25 days
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• Works independently to receive, triage and manage and reconcile adverse event reports, including those reported in the scientific literature, in accordance with contractual and regulatory timelines. • Works within multiple databases. Interact with clients, healthcare professionals, clinical trial personnel and consumers. • Reviews regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices, procedures and proposals. • Maintain medical understanding of applicable therapeutic area and disease states. May participate in on-call duties for specific projects to ensure 24-hr coverage of safety reporting. • Reviews cases entered for quality, consistency and accuracy, including review of peer reports. • Prepares and maintains regulatory and safety reports. • Assists with routine project implementation and coordination (e.g., Clinical trials, Endpoint Assessment Committee/Data Safety Monitoring Committee), including presentations at client/investigator meetings, and review of metrics and budget considerations. • Process reports for new clinical trial drug under Biogen. • Had been doing triage, serious and non-serious case processing and Quality Control (QC) for Fampridine team since Feb 2017 • Had been a part of core triage for post market and clinical trial reports non-serious/serious case
$15 USD in 40 days
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