Thane Maharashtra Drug regulatory Jobs – 11 Open Jobs Today

Medical Writer 1
IQVIA —Thane District, Maharashtra
- Doctoral degree
- Computer literacy
- Master's degree
13h
Clinical Operations Partner Lead
Bayer —Thane District, Maharashtra
- Call employer
- Bachelor's degree
Executive - Business Development (Pharma Testing Services)
Cotecna Life Science India Pvt. Ltd —Thane District, Maharashtra
- ₹5,00,000 - ₹5,50,000 a year
- Full-time
- Sales
- Business development
- Bachelor's degree
- Health insurance
- Life insurance
Quick apply
Pharmacy Assistant Professor of Medicinal Chemistry
St Wilfred's institute of Pharmaceutical Science & Research —Thane District, Maharashtra
- ₹30,000 - ₹60,000 a month
- Full-time
- Doctoral degree
- Laboratory experience
- Master's degree
Quick apply
12d
Senior Executive-QA
Piramal Enterprises —Thane District, Maharashtra
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
Manager - Regulatory Affairs
PolyPeptide Group —Amarnath, Maharashtra
- Master's degree
- Bachelor's degree
- APIs
Senior Executive - Production
Piramal Enterprises —Thane District, Maharashtra
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
Senior Executive
Piramal Enterprises —Thane District, Maharashtra
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
Manager - Quality Assurance
Piramal Enterprises —Thane District, Maharashtra
- Full-time
- APIs
Head Legal BP Pharma, CH, Radiology India
Bayer —Thane District, Maharashtra
- Call employer
- English
- Analysis skills
- Bachelor's degree
Manager - Supply Chain
PolyPeptide Group —Amarnath, Maharashtra
- Full-time
- ERP systems
- Master's degree
- Analysis skills

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Clinical Operations Partner Lead
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Accountable for applicable Phase I to IV studies' as well as Oncology and Cell & Gene Therapy studies’ monitoring, site management resources and activities in…
Manager - Quality Assurance
Piramal Enterprises —Thane District, Maharashtra
This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial…

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Medical Writer 1

IQVIA -
Thane District, Maharashtra

Apply Now

Job details

13 hours ago

Qualifications

Doctoral degree
Computer literacy
Master's degree
Bachelor's degree
Clinical trials
Technical writing
Medical terminology
Communication skills

Full job description

Job Overview
Acts as a Lead Medical Writer on straightforward projects (e.g. simpler documents under standard timelines). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Negotiates timelines and discusses/resolves customer comments, with senior support as needed.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including GCP, along with developments and advances in drug development/medical and/or technical writing.

Essential Functions

Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer.
Manage day-to-day workload: identify project needs, track timelines and implement customer requests, keeping manager/senior staff abreast of progress on tasks and any potential problems with project work.
Attend project team meetings with or without other writers. Participate in/lead comments resolution or similar meetings with external customers.
May give simple presentation to an existing customer (e.g. on processes at a Kick-off meeting).
Complete project finance activities, including monitoring and forecasting budgeted hours.
Awareness of budgets and project finance principles, moving towards review and understanding of budgets relating to assigned projects, including out of scope activities.

Qualifications

Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field Req
Master's Degree Master's Degree in life sciences related discipline or related field Pref
Ph.D. Ph.D. in life sciences related discipline or related field Pref
Typically requires 1-3 years of prior relevant experience and related competency levels. Req
Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.

Req

Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.

Req

Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output Pref
Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner. Req
In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas. Req
Excellent written and oral communication skills including grammatical/technical writing skills.
Excellent attention to detail and accuracy.
Communicates clearly, effectively and confidently with others.
Demonstrated abilities in collaboration with others and independent thought.
Demonstrates confidence and maturity in most routine medical writing situations.
Demonstrates good judgement in requesting input from senior staff.
Ability to establish and maintain effective working relationships with coworkers, managers and customers.
Ability to effectively manage multiple tasks and projects.
Must be computer literate.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

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drug regulatory jobs in thane maharashtra

Medical Writer 1

Clinical Operations Partner Lead

Executive - Business Development (Pharma Testing Services)

Pharmacy Assistant Professor of Medicinal Chemistry

Senior Executive-QA

Manager - Regulatory Affairs

Senior Executive - Production

Senior Executive

Manager - Quality Assurance

Head Legal BP Pharma, CH, Radiology India

Manager - Supply Chain

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