Remote Clinical data management Jobs – 55 Open Jobs Today

Clinical Trial Coordinator
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- English
1d
Clinical Data Manager-India
Indero —Remote
- Remote
- Microsoft Excel
- B.Sc
- English
- Work from home
- Flexible schedule
Quick apply
1d
Senior Clinical Data Associate (Rave)
Syneos - Clinical and Corporate - Prod —Remote
- Full-time
- Remote
- Microsoft Word
- B.Sc
- Windows
Medical Scientist
Syneos - Clinical and Corporate - Prod —Remote
- Full-time
- Remote
- Project management
- Data entry
8d
Sr Clin Data Team Lead
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Analysis skills
- Bachelor's degree
Senior Clinical Data Manager-India
Indero —Remote
- Remote
- Microsoft Excel
- B.Sc
- English
- Flexible schedule
Quick apply
11d
Production Support Analyst
Endpoint Clinical —Remote
- Weekend availability
- Hybrid work
- B.Sc
- Databases
- SQL
Data Surveillance Analyst
Parexel —Remote
- Remote
- Microsoft Office
- SQL
- Communication skills
Clinical Operations Lead (Clinical Trial Manager) (India)
Alimentiv —Remote
- Email
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
Quick apply
Business Analyst (Healthcare Domain)
HelixBeat —Remote
- Full-time
- Remote
- HIPAA
- Databases
- Analysis skills
- Health insurance
- Work from home
Quick apply
2d
Sr.Stat programmer clin pharm
Syneos - Clinical and Corporate - Prod —Remote
- Full-time
- Remote
- English
- Travel
- Communication skills
Ops Manager
ZenOnco.io —Remote
- ₹25,000 - ₹30,000 a month
- Full-time
- Remote
- Microsoft Excel
- Microsoft Office
- Master's degree
- Cell phone reimbursement
- Work from home
Quick apply
6d
Medical Writer (India)
ProductLife Group —Remote
- Remote
- Medicine
- Master's degree
- Analysis skills
Software Quality Engineer II
Clario —Remote
- Full-time
- Computer Science
- English
- Analysis skills
- Health insurance
3d
System Analyst
FuGenTex Solutions Pvt . Ltd —Remote
- ₹80,000 - ₹90,000 a month
- Full-time
- Remote
- SQL
- Analysis skills
- APIs
- Health insurance
Quick apply
5d
Software Quality Engineer
Clario —Remote
- Full-time
- Computer Science
- English
- Analysis skills
- Health insurance
1d
Virtual Registered Nurse (RN) – Post-Visit Patient Outreach
Cybersmart Technologies —Remote
- From ₹30,000 a week
- Full-time
- Remote
- English
- Care plans
- Communication skills
Quick apply
2d
Healthcare Software Planner
Siemens Healthineers —Remote
- Full-time
- Remote
- Software troubleshooting
- Master's degree
- Bachelor's degree
Quick apply
8d
AI Trainer – Pharmacists
Destinare services —Remote
- From ₹50,000 a month
- Remote
- Doctoral degree
- Bachelor's degree
- AI
- Flexible schedule
Quick apply
3d
Senior Medical Writer
Parexel —Remote
- Remote
- Microsoft Word
- Medicine
- Microsoft Excel

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clinical data management jobs near remote

Clinical Trial Coordinator

Thermo Fisher Scientific -
Remote

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Job details

Full-time
1 day ago

Qualifications

Microsoft Powerpoint
Microsoft Word
English
Local language
Microsoft Office
Presentation skills
Bachelor's degree
Organisational skills
Clinical trials
Computer skills
Diploma

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior 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 Senior Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting as a cross-functional liaison for the project team. You will act as a buddy during the onboarding phase and provide training to new staff as needed. Additionally, you will support departmental and cross-functional initiatives for process improvements and enhancements.

What You’ll Do:

According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate.
Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system.
Provides system support (i.e. GoBalto & eTMF).
Supports RBM activities.
Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
Supports scheduling and organization of client and/or internal meetings with completion of related meeting minutes.
Reviews and tracks local regulatory documents.
Transmits documents to client and centralized IRB/IEC.
Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
Maintains vendor trackers.
Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
Assists with study-specific translation materials and translation QC upon request.
May attend Kick off meeting and take notes when required.

Education and Experience Requirements:

High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
Bachelor's degree preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Ability to work in a team or independently as required
Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support 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
Excellent English language and grammar skills and proficient local language skills as needed
Good presentation skills
Excellent 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 PPD clinical training program
Self-motivated, positive attitude with effective strong interpersonal skills

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

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