Cbd Belapur Navi Mumbai Maharashtra Clinical data Jobs – 62 Open Jobs Today

Clinical Trial Coordinator - (FSP )
Thermo Fisher Scientific —Mumbai, Maharashtra
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- English
Head Quality Assurance-Clinical Research
Expecto Health Science —Kharghar, Navi Mumbai, Maharashtra
- ₹8,00,000 - ₹20,00,000 a year
- Full-time
- Management
- Research
- Master's degree
- Health insurance
- Paid time off
Quick apply
14d
Clinical Research Coordinator I - India
Iterative Health —Mumbai, Maharashtra
- ₹12,00,000 - ₹17,00,000 a year
- English
- Research
- Microsoft Office
Quick apply
Randomization & Study Product Coordinator
Medpace, Inc. —Navi Mumbai, Maharashtra
- Full-time
- Microsoft Excel
- Bachelor's degree
- Health insurance
- Paid time off
Clinical Research - Infection control
Thermaissance —Mumbai, Maharashtra
- ₹50,000 - ₹70,000 a month
- Part-time
- Medicine
- B.Sc
- Master's degree
Quick apply
12d
Clinical Data Svs Associate
Accenture —Mumbai, Maharashtra
- Full-time
- Master's degree
- Bachelor's degree
Clinical Pharmacologist
HRDR —Mumbai, Maharashtra
- ₹4,00,000 - ₹7,00,000 a month
- Full-time
- Medicine
- Doctoral degree
- In-person
Quick apply
Junior Data Engineer
Medpace, Inc. —Navi Mumbai, Maharashtra
- Full-time
- Azure
- Computer Science
- Databases
- Health insurance
- Paid time off
TL-Medical Safety
Cognizant —Mumbai, Maharashtra
- Full-time
- Hybrid work
- Research
- Analysis skills
- Travel
- Health insurance
Clinical Specialist / Stroke Rater – Punjabi Speaking
IQVIA —Mumbai, Maharashtra
- Part-time
- Remote
- Medicine
- Doctoral degree
- Master's degree
- Work from home
Executive-Production
Piramal Pharma Limited —Navi Mumbai, Maharashtra
- Full-time
- APIs
- Training & development
2d
Research Scientist-ADL
Piramal Pharma Limited —Navi Mumbai, Maharashtra
- Full-time
- APIs
9d
Medical Advisor, Ideation & Portfolio Development
Dr Reddy's Laboratories Limited —Mumbai, Maharashtra
- Full-time
- Medicine
- Doctoral degree
- Databases
- Health insurance
Quick apply
1d
PV Scientist - Case Processing
Soterius —Mumbai, Maharashtra
- Full-time
- Data entry
8d
SENIOR MEDICAL CODING PROFESSIONALS
scymes services pvt limited —Andheri, Mumbai, Maharashtra
- ₹30,000 - ₹50,000 a month
- Full-time
- Bachelor's degree
- In-person
- Medical terminology
Quick apply
3d
Clinical Research Medical Advisor
Novartis —Mumbai, Maharashtra
- Full-time
- Medicine
- Doctoral degree
- Bachelor's degree
6d
Data Scientist
Crosscope —Mumbai, Maharashtra
- Full-time
- Computer science
- AWS
- Machine learning
Clinical Specialist / Stroke Rater – Bengali Speaking
IQVIA —Mumbai, Maharashtra
- Part-time
- Remote
- Medicine
- Doctoral degree
- Master's degree
- Work from home
14d
Medical Records Manager
Progenesis IVF —Thane, Maharashtra
- Full-time
- Microsoft Office
- Bachelor's degree
- Organisational skills
- Health insurance
Quick apply
1d
Neuroscience CTM
Thermo Fisher Scientific —Mumbai, Maharashtra
- Full-time
- Microsoft Outlook
- English
- Bachelor's degree
12d

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Clinical Trial Coordinator - (FSP )

Thermo Fisher Scientific -
Mumbai, Maharashtra

Apply Now

Job details

Full-time

Qualifications

Microsoft Powerpoint
Microsoft Word
Project coordination
English
Local language
Microsoft Office
Bachelor's degree
Organisational skills
Clinical trials
Computer skills
Communication skills
Negotiation

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Trial Coordinator – 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.

As part of our global team, you’ll have the opportunity to provide administrative and technical support to the Project Team. As a Clinical Trial Coord, you'll support audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document. You will provide administrative support for site activation activities and aid in the development of the critical path for site activation within assigned projects to support rapid site activations. Representing CRG personnel, you may utilize local knowledge, organization systems, external site lists, and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. Additionally, you may act as a buddy during the onboarding phase and provide training to new staff as needed.

What You’ll Do:

Provide support for critical day-to-day clinical study activities, including regulatory inspection readiness, in accordance with established protocols under the general supervision of the Functional Service Provider (FSP) Manager and in collaboration with Client Management
Collaborate with Clinical Operations/Study Manager, study teams, and Clinical Research Organizations (CROs) to support clinical study activities as defined by the clinical trial operating model.

Review of study documentation, including essential document packets, study plans, informed consent forms, etc.
Supporting/oversight of risk-based monitoring.
Attendance of key team meetings as required, including Minutes for selected studies
Supporting regulatory inspection readiness (e.g. SOP Lists, storyboard collation.)
Support clinical trial systems (e.g. CTMS/TMF associated activities for selected studies
Supporting vendor contract administration as required.
Support study close-out activities, e.g. financial reconciliation
Supporting additional ad-hoc activities as needed, as agreed with Manager(s).

Education and Experience Requirements:

- Bachelor's degree preferred.
2+ years’ experience in global clinical trial support as a CTC / CTC / Project Coordinator
Experience in Phase 2 and 3 studies and global/international studies is advantageous.
Experience working across multiple therapeutic areas (including oncology) is advantageous
Have experience in Veeva Vault, Hands on experience in eTMF life cycle

Knowledge, Skills and Abilities:

Ability to work in a team or independently as required
Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Flexibility to reprioritize workload to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
Good English language and grammar skills and proficient local language skills as needed
Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
Ability to successfully complete the organizations clinical training program
Self-motivated, positive attitude and good interpersonal skills
Effective oral and written communication skills
Good interpersonal skills
Essential judgment and decision-making skills
Capable of accurately following project work instructions
Good negotiation skills
Independent thinker
Ability to manage risk and perform risk escalation appropriately

Working Conditions and Environment:

Work is performed in an office/ laboratory/clinical/ and/or home office environment with exposure to electrical office equipment.
Occasional drives to site locations. Potential Occasional travel required.

Apply Now

Refine Your Search

clinical data jobs in cbd belapur navi mumbai maharashtra

Clinical Trial Coordinator - (FSP )

Head Quality Assurance-Clinical Research

Clinical Research Coordinator I - India

Randomization & Study Product Coordinator

Clinical Research - Infection control

Clinical Data Svs Associate

Clinical Pharmacologist

Junior Data Engineer

TL-Medical Safety

Clinical Specialist / Stroke Rater – Punjabi Speaking

Executive-Production

Research Scientist-ADL

Medical Advisor, Ideation & Portfolio Development

PV Scientist - Case Processing

SENIOR MEDICAL CODING PROFESSIONALS

Clinical Research Medical Advisor

Data Scientist

Clinical Specialist / Stroke Rater – Bengali Speaking

Medical Records Manager

Neuroscience CTM

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