Basic qualifications: 6+ months of experience in Regulatory Writing Medical Writing and ICH Guideline. M.Pharm M. Sc in Micro Biology Responsibilities: Contributes to documents and activities to be included in registration files. Authors clinical documents following defined templates. Ensures the consistency and quality level of all documents that are issued. Actively participates in all planning, coordination and review meetings. Ability to work on 23 assignments simultaneously. Proactively raises and discusses concerns issues in an open and timely manner and within the global team at GSK Vaccines, thereby demonstrating the ability of promoting high scientific standards by pointing out obvious flaws and proposing and advocates alternatives. Works directly with diversity of roles at different levels within GSK e.g., Clinical Research and Development Leader CRDL, Project Level CRDL, Regional Medical Directors and Advisors, Study Delivery Leads SDL, Study Data Managers SDM, Biostatisticians, other Scientific Writers. Establishes network of communication and continuously builds collaboration to facilitate smooth partnerships and interfaces between all groups involved in delivery of writing assignments. LIGSK Our goal is to be one of the world?s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing. Important notice to Employment businesses Agencies GSK does not accept referrals from employment businesses andor employment agencies in respect of the vacancies posted on this site. All employment businessesagencies are required to contact GSK's commercial and general procurementhuman resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement verbal or written between the employment business agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment businessagency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businessesagencies in respect of the vacancies posted on this site. It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way. GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals entities in connection with recruitment with any GlaxoSmithKilne or GSK group company at any worldwide location. Even if they claim that the money is refundable. If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in ?gsk.com?, you should disregard the same and inform us by emailing askusgsk.com, so that we can confirm to you if the job is genuine.
5 lakhs to 12 lakhs per annum
Our?Pharmaceuticals business?has a broad portfolio of innovative and established medicines in respiratory, HIV, immuno-inflammation and oncology. We are strengthening our R&D pipeline through a focus on immunology, human genetics and advanced technologies to help us deliver transformational new medi...