Raipur Kalan Chandigarh Data entry associate Jobs – 16 Open Jobs Today

Patient Safety Associate II / Patient Safety Specialist
Parexel —Mohali, Punjab
- Nursing
- Microsoft Office
- Databases
10d
Fresher Accounts Associate - US Accounting
Cargaison Logistics Express Pvt Ltd —Mohali, Punjab
- ₹25,000 a month
- Full-time
- Microsoft Excel
- Accounting
- In-person
- Commuter assistance
- Health insurance
Quick apply
Medical Billing Associates
IDS-Argus Healthcare Services —Mohali, Punjab
- Night shift
- English
- Analysis skills
- Data entry
Associate Team Lead
Eventrics Multi Tasking Solutions Pvt Ltd —Chandigarh, Chandigarh
- ₹14,00,000 - ₹15,00,000 a year
- Part-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
Quick apply
3d
Front Office Associate
The Altius,Hotel —Chandigarh, Chandigarh
- ₹14,000 - ₹18,000 a month
- Full-time
- Customer service
- Word processing
- Administrative experience
- Food provided
Quick apply
Admin & Accounts Associate
Unienrol Guru Tech Private Limited —Chandigarh, Chandigarh
- From ₹25,000 a month
- Email
- Microsoft Excel
- English
- Microsoft Office
- Food provided
- Paid sick time
Quick apply
Insurance Process Associate
Auswide Pvt.Ltd —Mohali, Punjab
- ₹30,000 - ₹35,000 a month
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Finance
- Commuter assistance
- Health insurance
Quick apply
6d
Senior Associate Front Office
The Altius,Hotel —Chandigarh, Chandigarh
- ₹16,000 - ₹22,000 a month
- Full-time
- Customer service
- Word processing
- Administrative experience
- Food provided
Quick apply
10d
Data Entry Associate
Sprinzo Developerz —Mohali, Punjab
- From ₹8,000 a month
- Full-time
- Microsoft Word
- Microsoft Excel
- 12th Pass
- Paid time off
Quick apply
Sr. Business Development Associate
smartData Enterprises —Mohali, Punjab
- ₹50,000 - ₹1,50,000 a month
- Full-time
- In-person
- AI
- SDLC
- Health insurance
- Life insurance
Quick apply
Business Development Associate-(Bilingual: English/Spanish)
Dental Outsource Pvt. Ltd. —Mohali, Punjab
- ₹30,000 - ₹45,000 a month
- Full-time
- Bilingual
- Spanish
- English
- Commuter assistance
- Health insurance
Quick apply
Data Entry Executive
Purminder Kaur and Associates —Mohali, Punjab
- Up to ₹12,000 a month
- Email
- Walk-in
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Process Associate
Cogneesol —Mohali, Punjab
- Night shift
- Administrative experience
- Data entry
- Communication skills
Quick apply
9d
Charted Accountant
BK Nexus Enterprises —Mohali, Punjab
- ₹14,00,000 - ₹15,00,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
- Health insurance
- Life insurance
Quick apply
1d
Telecaller Sales Executive
Countryside Heaven private limited —Mohali, Punjab
- ₹20,000 - ₹30,000 a month
- Full-time
- Microsoft Word
- CRM software
- Microsoft Excel
Quick apply
BDG – Enterprise Sales
smartData Enterprises —Mohali, Punjab
- Azure
- DevOps
- Java

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Patient Safety Associate II / Patient Safety Specialist

Parexel -
Mohali, Punjab

Apply Now

Job details

10 days ago

Qualifications

Nursing
Clinical research
Regulatory reporting
Microsoft Office
Databases
Quality assurance
Bachelor's degree
Data entry
Pharmacy
Clinical trials
Communication skills
Time management

Full job description

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose – moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®.

About the Role

We are seeking a Patient Safety Associate II/Specialist to join our Patient Safety Operations team in a Temporary assignment (Contract role for 9 months) for on-site capacity. As a Patient Safety Associate II/Specialist, you will support global pharmacovigilance activities that advance new treatments for patients. This position plays a key role in safety case processing, regulatory submissions, literature surveillance, and compliance with international regulations. You will collaborate with cross-functional teams, follow industry-standard processes, and contribute to safety operations from study initiation through closeout.

Responsibilities include processing safety reports, executing regulatory submissions, conducting literature reviews, coordinating with affiliates, and supporting regulatory intelligence activities. You will join a fast-paced, growth-oriented environment focused on making a meaningful impact through ensuring patient safety and regulatory compliance. With diverse teams and continuous learning opportunities, the Patient Safety Associate II/Specialist can explore career paths and expand skills across global pharmacovigilance and clinical research.

Key Responsibilities

Monitor, process, and assess incoming safety reports from various sources, performing data entry and quality validation to ensure accuracy and compliance with regulatory standards
Execute safety case processing workflows including MedDRA coding, causality assessment, expectedness determination, and preparation of case documentation and narratives
Execute ICSR and periodic report submissions to regulatory authorities, maintaining compliance with global reporting timelines and regulatory requirements
Implement literature search strategies, screen publications for adverse drug reactions, identify potential safety signals, and maintain alignment with global pharmacovigilance regulations
Support communication and coordination between global safety operations and local affiliates, assisting with local health authority interactions and country-specific pharmacovigilance requirements
Conduct quality assurance activities, perform data reconciliation, and participate in metrics collection and reporting to support continuous improvement initiatives
Manage regulatory applications and product lifecycle changes in safety databases, supporting global regulatory activities across multiple regions
Research and disseminate regulatory intelligence to internal teams and clients, maintaining a centralized repository of regulatory updates and contributing to development of standard operating procedures
Collaborate with cross-functional teams and clients, attending meetings and coordinating activities to ensure timely delivery of safety deliverables
Develop and maintain knowledge of safety profiles, labeling, global regulations, and internal procedures while following documentation and archiving standards

You'll thrive in this role if you bring:

Strengths in analytical thinking, problem-solving, and attention to detail
Experience working in pharmaceutical, healthcare, or a regulated environment
The ability to collaborate across teams and communicate clearly with internal and external stakeholders
A patient-focused mindset and commitment to quality and regulatory compliance
Comfort working with pharmacovigilance systems, databases, and MS Office applications
Strong organizational and time management capabilities with the ability to manage multiple priorities

Required Qualifications

Bachelor's degree in Pharmacy, Nursing, Life Sciences, Health Sciences, or other health-related field (e.g., Biomedical Sciences, Microbiology, Biochemistry, Biotechnology, Dentistry), or equivalent qualification/work experience
2+ years of experience in safety case management, regulatory reporting, or pharmaceutical/healthcare environments
Knowledge of ICH-GCP guidelines, regional pharmacovigilance requirements, and clinical trial processes
Proficiency with safety databases and data analysis tools
Strong communication, organization, and problem-solving skills

Preferred Qualifications

Advanced degree or professional certification in pharmacovigilance or regulatory affairs
Experience with EudraVigilance, eCopy, or other pharmacovigilance systems
Familiarity with regulatory submission processes and portal/gateway systems
Experience in a global or multi-regional pharmacovigilance environment

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.

If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply!

Apply Now

Refine Your Search

data entry associate jobs in raipur kalan chandigarh

Patient Safety Associate II / Patient Safety Specialist

Fresher Accounts Associate - US Accounting

Medical Billing Associates

Associate Team Lead

Front Office Associate

Admin & Accounts Associate

Insurance Process Associate

Senior Associate Front Office

Data Entry Associate

Sr. Business Development Associate

Business Development Associate-(Bilingual: English/Spanish)

Data Entry Executive

Process Associate

Charted Accountant

Telecaller Sales Executive

BDG – Enterprise Sales

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