Search Results: 7,631 vacancies
...studies with the available/existing published research and highlight important points... ...Design and Planning
Develop and design clinical research protocols for holistic healthcare... ...activities comply with ethical standards, regulatory requirements, and industry best practices...
...We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator,... ...successful execution of research protocols in accordance with regulatory requirements and ethical standards.
Responsibilities:
Coordinate...
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements...
...Technical Requirements of Pharmaceuticals for Human Use (ICH) / Good Clinical Practice (GCP), local regulations and Standard Operating... ...and CRA Managers as well as Medical Science Liaisons, Clinical Research Medical Advisors (CRMA) and medical advisors to ensure optimal recruitment...
...accordance with study protocol and applicable regulatory requirements
Work with CROs to adapt,... ...to monitoring and study plan
Support clinical quality in managing CAPAs and other study... ...in clinical trials industry as Clinical Research Associate
Good working knowledge of...
Allergan's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology...
Description
Manager- Clinical research & Performance Assessment
Skill
Clinical research,Performance Assessment , Personal care, new product, innovation
Qualification
~ Design and conduct clinical trials in the skin category such as Acne, Pigmentation, Atopic Dermatitis, Skin hydration, Skin Barrier function & Anti-ageing.
~ Co-ordinate with product development team to understand the product benefits & develop robust study design & protocol...
...Position: Clinical Documentation Specialist
Grade: 12
Reporting To: Team Manager
Department: CARE - Virtual Scribe
Profile Description: This role would be responsible for creating medicolegally compliant, clinically sound, high quality outpatient visit documentation...
...Description
The Position
This role is accountable for regulatory medical writing (RMW) to support Organon’s clinical development programs.
Provide medical writing... ...authoring platform.
Participates in Clinical Research Organization (CRO) alliance and other outsourcing...
...Company Name: FashionTV.
Location: Mumbai Santacruz (West)
Designation: Research and Development Specialist
About Company:
FashionTV a global leader in fashion media and lifestyle boasts over 25 years of excellence. Recognized for empowering entrepreneurs FashionTV...
...collaborates with the Trial Monitoring Organisation to ensure fast clinical trial start up, recruitment according to planned timelines,... ...interaction (or local Board of Health) as required
• Support Regulatory Affairs, Health Economics, Drug safety and epidemiology and Medical...
...Role - Clinical Database Programmer Location - Mumbai
• A person should have 6 - 10 years of experience in Medidata RAVE Custom Function
Programming.
• Should have good knowledge and understanding of Object-Oriented Programming
concepts.
• Should have good knowledge...
...Job Title
MR Clinical Application Specialist
Job Description
About the Organization Rated amongst the Top 50 Great Places to Work, Philips Healthcare in India operates in the medical equipment and diagnostic imaging segment including CT, MRI, Xrays, cardiovascular...
...critical role in powering economic growth globally. The Equity Research department provides independent and objective market analysis to... ...internal functions and in accordance with company policies and regulatory changes.
Manage work priorities considering market timelines...
...We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.
Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory Affairs
Experience: 3 to 9 years
Location: Andheri...
...highly motivated and technically proficient Product Application Specialist to join our Point of Care (POC) business unit. As a 'Product... ...activities, conducting sales demos, engaging with customers in clinical settings, and handling technical escalations or product service...
...for all statistical tasks on the assigned clinical trials: clinical trial design and... ...requirements (SOPs, Master Analysis Plan, GCP, and regulatory guidelines).
- Should participate in... ..., Good Manufacturing Practices, Clinical research, and clinical trials process and related...
...serving the Cybersecurity industry by offering news, views, and research all focused on the top topics faced by professionals in the... ...Opportunity
ISMG is currently seeking a Data Mining and Research Specialist who will assist in researching and updating various aspects of...
...ensure compliance with all product stewardship communications and regulations.
To liaise with stakeholders to identify forthcoming regulatory challenges and proactively seek expert input to resolve issues for ensuring continuity of market access to Indorama Ventures Oxides...
