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Career as Pharma Data Entry Associate at Accenture

Accenture is a global management consulting, technology services and outsourcing company, with approximately 275,000 people serving clients in more than 120 countries. Combining unparalleled experience, comprehensive capabilities across all industries and business functions, and extensive research on the world’s most successful companies, Accenture collaborates with clients to help them become high-performance businesses and governments. The company generated net revenues of US$28.6 billion for the fiscal year ended Aug. 31, 2013.

Post: Pharma Data Entry Associate


Vacancy at Novo Nordisk as GCP Lead Auditor - Degree in pharmaceutical or natural science

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

Post: GCP Lead Auditor


Application invited from eligible candidates for post of Sr. Clinical Process Associate in Quintiles

Quintiles is the only fully integrated biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. Our network of 23,000 engaged professionals in 60 countries around the globe works with an unwavering commitment to patients, safety and ethics — ensuring a higher level of healthcare for people. For our biopharmaceutical customers, we help them navigate risk and seize opportunities in an environment where change is constant.


Required for Clinical Data Analyst in Theorem

When you think about it, your perfect research partner is the one who gives you an edge: people who have just that extra bit of knowledge or expertise to see a fresh angle to simplify a complex clinical trial. Your perfect research partner is a group of accomplished professionals with deep therapeutic expertise and a passion for research. Your perfect research partner is a worldwide organization that’s big enough to handle comprehensive global trials but small enough to pay meticulous attention to a single-site study. Your perfect research partner is Theorem.

Post: Clinical Data Analyst


Vacancy in Institute of Good Manufacturing Practices India for posts of Assistant Professor | M.Pharma / M.Sc / Ph.D may apply

Institute of Good Manufacturing Practices India, registered as a non-profit society (under Societies Registration Act, 1860) with Government of India and a member (as a higher/professional education Institute) of Quality Council of India (QCI), Government of India -presents unique, friendly and interactive platform to get rid of all your GMP related glitches. GMP- is an essential and most dynamic element of industries like pharmaceutical, Biotechnology, cosmetic, Ayurveda, Homeopathy, medical device and food manufacturing. Keeping self-updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices. With its mission of "Knowledge Dissemination and Human Resources Development in pharma, food and healthcare Industries", IGMPI is moving hand in hand with technology advances and has gained recognition as global training provider for pharma, healthcare, food & nutrition and agriculture professionals and students in the mentioned areas. The Institute has various faculties like Faculty of Food Safety and Quality, Faculty of GMP, Faculty of Clinical Research, Faculty of Healthcare Administration, Faculty of Intellectual Property Rights, Faculty of Nanotechnology, Faculty of Product Management and Academy of Medical Coders India. The courses have been structured and designed under the guidance of field experts and thus promise to impart theoretical and practical knowledge about the defined subjects. Based on high standard of quality, the training programmes have been duly approved and certified by Quality Council of India, Government of India. (www. igmpiindia.org | www. amciindia.org | www. ffsqindia.org | www. fcrindia.org | www. fhaindia.org )

Post: Assistant Professor (Multiple posts)


Vacancy in Parexel for Associate Project Manager

PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.


Work as Clinical Data Coordinator in Icon Clinical Research

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

Post: Sr.Clinical Data Coordinator


Job as Senior Clinical Process Associate in Quintiles

Quintiles is the only fully integrated biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. Our network of 23,000 engaged professionals in 60 countries around the globe works with an unwavering commitment to patients, safety and ethics — ensuring a higher level o f healthcare for people. For our biopharmaceutical customers, we help them navigate risk and seize opportunities in an environment where change is constant.

Post: Sr Clin Prcess Assoc, Clin GDN-1524781


Required for Manager, Document Management in Icon Clinical Research

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

We are currently looking to strengthen our growing Document Management team in the recruitment of a  Manager, Document Management individual.

Post: Manager, Document Management


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