13 Biopharmaceutical Leadership jobs in Remote - Republic of India.

Hiring now: Medical Writer Ii Clinica @ Syneos Hea, Sr Clinical Data Analyst @ Parexel, Analyst Ii Global Data Mg @ Johnson Jo, Sr Principal Statistical @ Novartis, Principal Biostatistician @ Iqvia.Explore more at jobswithgpt.com.

🔥 Skills

medical writing (3) Biostatistics (3) quality control (3) project management (3) regulatory guidelines (3) FDA regulations (2) Clinical Trials (2) Data Management (2) Clinical Research (2) Functional Service Provider (2)

📍 Locations

Republic of India (13)

Syneos Health

Skills & Focus: clinical study protocols, clinical study reports, medical writing, statistical analysis plans, regulatory standards, clinical literature searches, FDA regulations, ICH-E3 guidelines, peer reviewer, drug development process
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Type: Full-time

Parexel

Skills & Focus: Clinical Trials, Data Management, Biostatistics, Clinical Research, FSP, CRA, Functional Service Provider, Oncology, Statistical Programming, Epidemiology
About the Company: Parexel helps clients accelerate the development and commercialization of innovative new therapies with expertise in regulatory consulting, clinical trials, an…
Skills & Focus: Drug Safety, Pharmacovigilance, Adverse Events, Signal Detection, Safety Reports, Clinical Study Reports, Medical Review, International Drug Regulations, GCP, GVP
Experience: 3 Years
Skills & Focus: regulatory affairs, biologics, observation, guidelines, submission, collaboration, stakeholders, independently, regulatory framework, countries
Experience: 7-9 yrs
Benefits: Flexible work arrangements

Syneos Health

Skills & Focus: medical writing, clinical trial disclosure, regulatory requirements, quality control, clinical documents, protocol registration, anonymization, FDA regulations, ICH guidelines, clinical research
About the Company: We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build t…
Experience: 4-8 years
Benefits: Comprehensive benefits program encompassing total health - physical, mental and financial.

Parexel

Clinical Data Analyst Republic of India
Skills & Focus: Clinical Data, Data Management, Biostatistics, Clinical Research, Medical Trials, Statistical Programming, Project Leadership, Functional Service Provider, Clinical Operations, Health Improvement
About the Company: Parexel provides a range of services to the biopharmaceutical industry, specializing in clinical research.

Syneos Health

Skills & Focus: FDA, EU, medical writing, data integrity, copyediting, project management, medical standards, document accuracy, style guide, regulatory guidelines
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medica…
Salary: $55,800 to $108,600
Type: Full-time
Benefits: Health benefits include Medical, Dental, Vision, Company match 401k, eligibility to participate in Employee Stock Purch…
Principal Stat Programmer Republic of India
Skills & Focus: SAS, programming, statistical analysis, clinical trial, data listings, quality standards, CDISC Standards, regulatory guidelines, programming specifications, team collaboration
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…

Johnson & Johnson

Skills & Focus: data management, clinical data, healthcare, clinical trials, regulatory compliance, data analysis, stakeholders, project management, quality assurance, clinical development
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Approx. 2 years of experience in Pharmaceutical, CRO or Biotech industry or related field or industry.
Type: Hybrid
Benefits: We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority,…

Novartis

Skills & Focus: statistical programming, clinical studies, programmer, biostatistics, data structures, CDISC, quality control, timely deliverables, project-level strategies, validation of datasets
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Skills & Focus: technology, drug development, data collection, clinical data operations, automation, programming, data submission, analytics, KPIs, strategic vision
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives.

Iqvia

Principal Biostatistician Republic of India
Skills & Focus: Biostatistics, Statistical Analysis, Data Communication, Regulatory Submission, SAS, R Programming, Oncology, Clinical Trials, Quality Assurance, Independent Study Execution
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Ph.D. in Statistics or related field with minimum 3 years relevant experience, or Master’s in Statistics or related field with minimum 5 years of relevant experience.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novartis

Skills & Focus: clinical documents, regulatory guidelines, quality control, publishing consultancy, submission publishing, project management, time management, cross-functional teams, electronic publishing, regulatory affairs
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Experience: Experience with regulatory submission format, including familiarity with submission publishing activities and CTD format criteria.