Vacancies in Novartis
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Team Lead - Safety Processing Expert Group (Job ID: 31372BR)
(Postgraduate degree in Medicine / Pharmacy or Doctorate in Life Sciences or equivalent degree with at least 4 years experience in Pharmaceutical R&D, including at least 2 years in clinical safety or closely related areas of Development and at least 3 years management experience with demonstrated leadership skills)
Lead a team of medically trained safety processing experts
Manage, direct and control resources for the evaluation and consistent handling of Adverse Event Report workload
Ensure compliance with reporting timelines and review deliverables to maintain established quality standards
Strong leadership skills, knowledge of medicine and problem solving skills
Strong communication, interpersonal skills and good understanding of pharmacovigilance
process, requirements
Safety Processing Expert (Job ID: 31058BR)
(Postgraduate degree in Pharmacy / Life Sciences or graduates in Medicine from premier institutes, with at least 2 years experience in Pharmaceutical R&D / drug safety / pharmacovigilance. Fresh graduates / postgraduates in Medicine from premier institutes could also apply)
Facilitate safety monitoring by optimizing scientific quality documentation of safety case reports for Novartis drugs
Responsible for the receipt, tracking and initialization of single case drug safety reports in to the safety database
Responsible for accurate data entry and coding of Adverse Event reports and evaluation of non-expeditable reports within well defined timeframes, in compliance with IMS business rules, standard operating procedures and regulatory requirements
Lead CRO Manager (Job ID: 30105BR)
(Postgraduate degree in Life Sciences / Medical Science / Pharmacy or equivalent relevant degree with 7+ years in Drug Development in Pharma Industry, CRO, Central Lab / Speciality Provider)
Manage Contract Research Organizations (CROs), Central Labs / Reference Labs and Specialty Providers to assure delivery of quality, timely and cost-effective external resources to support Novartis Development pipeline
Provide strategic and operational Project Support & Business Intelligence for India and Asia Pacific
A solid understanding of clinical development process and management of clinical trials is required
Excellent negotiation skills are a must
Strong problem-solving skills, communjcation skills and interpersonal skills are key for this
position
Lead Statistical Analyst (Job ID: 30803BR)
(Ph.D / M.Phil in Statistics with 4+ years experience in clinical trials or M.Sc. (Statistics / Computer Science) with 6-8 years of experience in clinical trials)
To lead project level activities (statistics / programming) in all phases of clinical trials
Expert knowledge of statistical analyses in all phases of clinical trials
Expert knowledge and experience with statistical software (SAS, S-Plus)
Advanced knowledge of database design / structures
Expert Publication Writer (Job ID: 31336BR)
(Ph.D in Life Sciences / Applied Biology, MD in internal Medicine / Pharmacology, MBBS with 3-4 years experience in leading pharmaceutical / research companies, including medico-marketing, or academic institutions)
Disease / Therapeutic area expertise
Excellent communication and project managementskills
Publications in indexed journals / high quality scientific writing
Prepare high quality publications (manuscripts, abstracts, short communications, review articles, publication alerts), including slide presentations, posters, etc.
Liaise globally with internal and external contributors
Assist in publication planning and communication strategies in therapeutic areas
Group Head - Scientific Writing (JoblD:28218BR)
(Ph.D in Life Sciences / Applied Biology, MD in Internal Medicine / Pharmacology with 5-10 years experience in leading pharmaceutical / research companies, including medico-marketing, or academic institutions, with at least 3 years experience in a senior managerial position)
Excellent interpersonal & communication skills, project & matrix management skills and leadership skills
Publications in indexed journals and/or previous writing experience in safety documents (including narratives) and Clinical Study Reports (CSRs)
Expand and operationally manage Scientific Writing Groups for production of -
high quality pubiications (manuscripts, abstracts, short communications, review articles, publication alerts), including slide presentations, posters, etc.
high quality clinical documentation (e.g. Clinical Study Reports and Summary Documents) for submission to regulatory authorities
Group Head - Data Management (Job ID: 28306BR)
(Postgraduate degree in Life Sciences / Computer Science / Pharmacy or equivalent relevant degree with 7+ years in the discipline of Clinical Data Management)
Lead a team of Data Managers and operationally manage, direct and coordinate Clinical Data Management activities for global trials
Strong technical and problem solving skills, and ability to evaluate computer systems
for Clinical Data Management
Advanced knowledge of Clinical Development Processes and Drug Development
Group Head - eCRF Development (Job ID: 24038BR)
(Postgraduate degree in Life Sciences / Mathematics / Computer Science / Medical Informatics or equivalent degree with 7+ years in the discipline of Database Design / Programming)
Lead a team of eCRF Developers and operationally manage, direct and coordinate eCRF Development activities
Strong technical and problem solving skills, good understanding of database management systems and its application to eCRF Development and Electronic Data Management
Advanced knowledge of Clinical Development Processes & Drug Development