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Home
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Jobs in Bengaluru
>
Thepharmadaily
>
Senior Centralized

Senior Centralized

Thepharmadaily

2 - 5 years

3 - 7 Lacs

Bengaluru Karnataka India

Posted:1 day ago| Platform: Foundit logo

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Skills Required

ctms IWRS Sops CRAs

Work Mode

On-site

Job Type

Full Time

Job Description

Key Responsibilities

Standard Operating Procedures

Adhere to all applicable
Standard Operating Procedures (SOPs)
and
Work Instructions
relevant to departmental and study-specific activities.

Daily Operations

Perform
day-to-day operational tasks
, ensuring adherence to quality standards and maintaining productivity levels.

Metrics Tracking

Track and report metrics
as defined by management within required timelines.

Process Improvement

Participate in
process improvement initiatives
, assisting with the implementation of revised processes and procedures to enhance efficiency and compliance.

Study Management Support

Manage clinical systems
and oversee
access management
for study tools and platforms.
Handle and maintain
study documents
, supporting
electronic Trial Master File (eTMF)
management.
Maintain and update
study databases
(e.g.,
CTMS
,
IWRS
,
EDC
).
Assist the study team with
data review
and other
support activities
.
Track
and follow up with
Clinical Research Associates (CRAs)
regarding outstanding issues.
Generate
study-specific reports
to support decision-making and monitoring.
Manage
internal and external communications
to ensure alignment among stakeholders.
Ensure
training compliance
for all study team members.
Oversee
study payments
for clinical sites and vendors, ensuring accuracy and timeliness.

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