India Remote Clinical research Jobs – 49 Open Jobs Today

Research Associate III - Evidence Synthesis
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Doctoral degree
- Research
- Master's degree
Patient Safety Physician
Parexel —Remote
- Remote
- Medicine
- Doctoral degree
- Microsoft Office
2d
Clinical Trial Coordinator II - FSP
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- English
8d
Freelance – Delphi Study Cardio-Renal & Metabolic Disease (Clinical Research Expert)
Guires Solutions Private Limited —Remote
- From ₹10,000 a month
- Part-time
- Remote
- Doctoral degree
- Research
- Bachelor's degree
Quick apply
10d
Clinical Operations Lead (Clinical Trial Manager) (India)
Alimentiv —Remote
- Email
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
Quick apply
Prior Authorization Operations Manager (IN)
Squad Health —Remote
- ₹95,000 - ₹1,15,000 a month
- Full-time
- Remote
- English
- EMR systems
- AI
Quick apply
Oncology Data Specialist
CrescereMed —Remote
- ₹30,000 - ₹45,000 a month
- Full-time
- Remote
- Nursing
- English
- Data entry
- Work from home
Quick apply
14d
US Healthcare Tech Consultant / EHR Analyst
HoonarTek —Remote
- Part-time
- Remote
- Research
- SQL
- Agile
Senior Clinical Data Manager-India
Indero —Remote
- Remote
- Microsoft Excel
- B.Sc
- English
- Flexible schedule
Quick apply
Project Manager I
Clario —Remote
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
10d
Senior Director - Clinical
Intelehealth —Remote
- Full-time
- Remote
- Medicine
- Research
- Master's degree
- Health insurance
- Flexible schedule
Senior Manager, Clinical Operations (FSP )
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Research
- Bachelor's degree
8d
Sales Nutrition
Fitelo —Remote
- ₹18,000 - ₹25,000 a month
- Full-time
- Remote
- Sales
- Master's degree
- Bachelor's degree
- Paid time off
- Work from home
Quick apply
Senior Medical Writer & Evidence Analyst
Catalyst Clinical Research, LLC —Remote
- Full-time
- Remote
- Microsoft Word
- Medicine
- Doctoral degree
Medical Writer I /Medical Writer II (CSR Narratives)
Syneos - Clinical and Corporate - Prod —Remote
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
6d
Statistical Programmer, India
Indero —Remote
- Remote
- English
- Master's degree
- Bachelor's degree
- Flexible schedule
Quick apply
Regulatory Consultant (CMC-EU, GCC & AU)
Syneos - Clinical and Corporate - Prod —Remote
- Full-time
- Remote
PRINCIPAL MEDICAL WRITER
Catalyst Clinical Research, LLC —Remote
- Full-time
- Remote
- Microsoft Word
- Medicine
- Doctoral degree
Senior Clinical Database Programmer
Parexel —Remote
- Remote
- Java
- SQL
- Business development
6d
Statistical Programmer II (SDTM)
Parexel —Remote
- Remote
- Computer Science
- English
- Master's degree
13d

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Research Associate III - Evidence Synthesis

Thermo Fisher Scientific -
Remote

Apply Now

Job details

Full-time

Qualifications

Economics
Doctoral degree
Research
Master's degree
Bachelor's degree
Staff training
Computer networking

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join us as a Research Associate III (Evidence Synthesis) – Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

Position Overview:

This role will independently direct key aspects of systematic literature review (SLR) research projects with guidance from senior staff, as well as manage multiple projects with tasks varying to degree by project.

Essential Duties and Responsibilities:

Define and refine research questions as they pertain to the SLR objectives

Design of literature searches/algorithms to be implemented in scientific literature databases (i.e., PubMed, EMBASE, Cochrane Library, etc.) and grey literature sources (conference proceedings, regulatory agencies).

Develop inclusion/exclusion criteria within the PICOS framework to be implemented during screening process

Oversee the screening of abstracts and full-text articles against defined inclusion/exclusion criteria to assess their suitability for inclusion in the review

Review the PRISMA diagram depicting the study attrition

Validate data abstraction and extraction

Finalize the analyzable dataset

Draft tables and figures for analysis results

Synthesize the evidence base by through drafting and editing sections of project deliverables (e.g. reports, protocols, statistical analysis plans) and dissemination actives, abstract and manuscript preparation

Delegate tasks to junior staff and review their work as appropriate

Develop a project plan and monitor project progress, including timeline and budget

Draft project proposals, including scoping the body of evidence and preparing project budgets)

Co-lead (or lead) client communications, both via email, phone, and in-person; responsible for day-to-day communications

Participate in nonliterature-based research and consulting activities within other departments (e.g., modeling and simulation, real-world evidence).

Participate in staff recruitment and training efforts

Serve as a line manager (depending on skills/experience)

Education, Professional Skills & Experience:

PhD in health sciences, economics, biology, natural sciences or a related field with some related experience; MSc. with significant related experience, or Bachelors with extensive relevant experience.

Proven experience in systematic literature review methods in health economics and/or health services research; experience in network meta-analysis would be an advantage but is not essential.

Personal Skills & Competencies:

Commercial experience in a similar environment is highly desirable, but not essential

Deep understanding of research principles and demonstrated practical research implementation

Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

Frequently interacts with others to obtain or relate information to diverse groups.

Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals.

Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multitask.

Regular and consistent attendance.

Apply Now

Refine Your Search

clinical research jobs in india remote

Research Associate III - Evidence Synthesis

Patient Safety Physician

Clinical Trial Coordinator II - FSP

Freelance – Delphi Study Cardio-Renal & Metabolic Disease (Clinical Research Expert)

Clinical Operations Lead (Clinical Trial Manager) (India)

Prior Authorization Operations Manager (IN)

Oncology Data Specialist

US Healthcare Tech Consultant / EHR Analyst

Senior Clinical Data Manager-India

Project Manager I

Senior Director - Clinical

Senior Manager, Clinical Operations (FSP )

Sales Nutrition

Senior Medical Writer & Evidence Analyst

Medical Writer I /Medical Writer II (CSR Narratives)

Statistical Programmer, India

Regulatory Consultant (CMC-EU, GCC & AU)

PRINCIPAL MEDICAL WRITER

Senior Clinical Database Programmer

Statistical Programmer II (SDTM)

I want to receive the latest job alerts for clinical research in india remote

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