Clinical Study Report - Gurugram, Haryana

Clinical Study Report Writer · We are seeking an experienced Clinical Study Report (CSR) writer to develop high-quality clinical documentation for regulatory submissions. · Author, review and finalize CSRs for Phase I-IV studies. · Ensure compliance with ICH-E3 protocol and regul ...

We are seeking an experienced Clinical Study Report (CSR) Writer to develop high‑quality clinical documentation for regulatory submissions. · Author, review, and finalize Clinical Study Reports (CSRs) for Phase I–IV studies. · Ensure compliance with ICH‑E3, protocol, and regulato ...

The Clinical Safety Manager is responsible for ensuring appropriate safety review of documents including Investigator Brochures, Clinical Study Reports, and Aggregate Reports. The role involves reviewing adverse events, serious adverse events, and safety data from clinical studie ...

Responsibilities: · The purpose of this position is to Develop / Automate dashboards, Working on Decks, Generating Reports & Analysis, Support and assist in the management, Functional departments on Gathering & Working on Regular reports, and provide Ad-hoc reports. · Be the sing ...

About the Role · We are looking for a skilled Power System Engineer with handson experience in power system modelling, grid studies, and stability assessments for renewable energy (RE) projects, including hybrid configurations. The ideal candidate will have strong technical exper ...

Position Objective and Responsibilities · The candidate will be a key member of the Guardian India Actuarial Team, with ongoing partnership and support to the Strategic Initiatives and Inforce Management Team. · Key Responsibilities include: · Experience Studies · Lead and review ...

The candidate will work dedicatedly with an investment bank and will be responsible for end-to-end management of the projects. · ...

ReNew is one of the largest renewable energy companies globally with a leadership position in India. · ...

Position Purpose · The role holder shall report to the Lead Regulatory LATAM & Global Chemistry and shall be · responsible for: · Design, select, and oversee environmental fate and degradation studies in accordance · with international guidelines (e.g. OECD, EPA, IBAMA). · Provid ...

**Job Title: Site Coordinator** · **Responsibilities:** · 1. **Site Planning & Coordination:** Develop and implement site plans, ensuring alignment with project requirements and timelines. Coordinate with internal teams and external stakeholders to optimize site resources and act ...

The ideal candidate is serve as the lead marketing executive. You will manage all marketing efforts including planning, research, advertising, communications and public relations in line with our objectives. · Responsibilities · Lead end-to-end Meta strategy across traffic, aware ...

We are looking for a highly skilled and experienced Senior Clinical Research Associate to join our team in the Pharmaceutical and Life Sciences industry. The ideal candidate will have a strong background in clinical research and a proven track record of success in managing comple ...

Track New project/plant setup progress with focus on project milestones and timeline adherence. · Understand plant layout concerns reported during construction phase and study countermeasure plans with PE/Civil/Utility teams. · Prepare schedules, reports and review presentations. ...

Key Responsibilities: · Lead the design, development, and review of clinical study protocols and amendments. · Provide scientific leadership and guidance throughout the clinical trial lifecycle. · Collaborate with cross-functional teams including regulatory, biostatistics, ...

We are seeking an experienced Pharmacovigilance professional with strong expertise across drug development, registration and post-approval phases for New Chemical Entities (NCEs). The role will be responsible for end-to-end safety activities regulatory compliance signal managemen ...

The candidate will work dedicatedly with an investment bank and be responsible for end-to-end management of projects. · ...

This role involves preparing estimates and budgets, performing cost control and analysis, managing contracts, and handling quantity surveying for civil projects. · Experience in Cost Estimation Budgeting and Cost Analysis ...

Senior Manager Job Description · The Senior Manager leads and manages clinical trials from start to finish including planning initiation execution coordination oversight compliance reporting data analysis resource allocation budget management continuous improvement. · Responsibil ...

Design methodology and tools for data Collection · ...

Qualification -B.Tech (Electrical)/ B.E (Electrical) Or ME/M-Tech/M.Sc (Power/Electrical) · Job Description · Study of system study improvement in the power distribution system. · To prepare execute BU plan for the next 3 years in consultation with Top Management. · Monitor Proje ...