Prepare for Your Axis Clinicals Interview with Real Experiences!
View interviews
AmbitionBox
Search
Jobs
- Reviews
- Salaries
- Interview Questions
- About Company
- Benefits
- Jobs
- Office Photos
- Community
Add office photos
All Filters
9 Axis Clinicals Jobs
Clinical Research Associate - I
0-3 years
Warangal, Hyderabad / Secunderabad, Nizamabad
1 vacancy
Clinical Research Associate - I
Axis Clinicals
posted 3+ weeks ago
Job Role Insights
Fixed timing
Key skills for the job
Job Description
Essential Function:
The responsibility of a Clinical Research Assistant (CRA I) is to support the project team by documenting information concerning the progress of clinical trials such that it is always complete, up-to-date and available to team members and sponsors
To help communicate actions between Sponsor, project team members and to be viewed by the CRAs as an important source of project information and assistance
While assisting project team for assigned projects, Clinical Research Assistant (CRA I) learns how to monitor and develop an understanding of the drug development process, relevant regulations and AXIS SOPs
Relationships:
Reports to: Clinical Lead (CL) or Project Manager (PM)
Directly supervises: None
Provides work direction to: None
Works closely with: CRAs, Project Managers, Regulatory Affairs, Clinical Logistics, Finance
External relationships: Third party vendors
Responsibilities:
- Assists CRAs, CL, and PM with updation and maintainenance of multiple types of clinical tracking systems related to study team, site compliance, performance and study milestone achievement Assists the clinical team in the preparation, handling, distribution, filing, archiving of clinical documentation and reports according to the scope of work. Obtain any missing/incomplete data from investigators in conjunction with CRAs
- Prepares the correspondence to the site to send the study details, questionnaire and related matter to obtain the feedback as required
- Updates the Investigator s database on the regular basis
- Assists CRAs with preparation, handling, distribution of Clinical Trial Supplies and maintenance of tracking information
- Ensure CRF pages are being processed, tracked and forwarded to Data Management on time
- Performs assigned duties with direction from Project Manager, to assist team members with designated administrative tasks in support of clinical trial execution and management
- Prepare and submit or support those involved in regulatory and ethics committee submissions. Ensure that documents are collected in a timely manner in order to meet regulatory and ethics committee/IRB submission dates
- Assist with the preparation of presentations at investigator meetings
- Assist CRAs in their routine administrative tasks (e.g. metrics, arranging meetings and travel)
- Attend staff meetings and training sessions as required
- Completes appropriate protocol and fundamental clinical research training including the requirements of guidelines and applicable local regulations
- Performs administrative duties as directed
- Attend Observational Site Visits, determined by Project Manager
- Participate in project meetings (taking minutes if appropriate), replace CRAs on project team calls when necessary
- Have up to date knowledge on study procedures and study related materials, Responsible for completeness, quality, and accessibility of Central Files.
- Supervise receipt, tracking, and archiving of documents for Central Files
- Provide Clinical Lead and the team with detailed information on study procedures and study related materials
- Responsible for up to date reports of study status in CTMS or client equivalent tracking systems. Organise project meetings and take minutes
- Proactively flag any project related issues
Skills
Competent in written and oral English
Team player with outstanding negotiation and organizational skills
A flexible attitude with respect to work assignments, and new learning
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Willingness to work with multiple supervisors/colleagues in a matrix environment, and to value the importance of team work
IT literate (experience with Microsoft based applications and general knowledge of PC functions)
Education:
Educated to Bachelor s or Master s degree level (biological/ life science, pharmacy or other health related discipline preferred)
Language Skills:
Competent in written and oral English
Physical Requirements:
Ability to travel whenever required
Employment Type: Full Time, Permanent
Read full job description
What people at Axis Clinicals are saying
Rating based on 9 Clinical Research Associate
reviews
Anonymous · Other
in Hyderabad / Secunderabad
Likes
Best organisation for freshers
- Salary - Excellent
+6 more
Dislikes
Hahahaha Nothing major
Clinical Research Associate salary at Axis Clinicals
reported by
47
employees
with 1-6
years exp.
₹2
L/yr - ₹6.5
L/yr
13%
more
than the average Clinical Research Associate Salary in India
View more details
What Axis Clinicals employees are saying about work life
based on 119 employees
Strict timing
Alternate Saturday off
No travel
Day Shift
Axis Clinicals Benefits
View more benefits
Compare Axis Clinicals with
IQVIA
Compare
Syngene International
Compare
SGS
Compare
Aragen Life Sciences
Compare
SAI Life Sciences
Compare
Parexel International
Compare
ICON Plc
Compare
Fortrea Development India Private Limited
Compare
Aizant Drug Research Solutions
Compare
Veeda Clinical Research
Compare
Cliantha Research
Compare
MRO
Compare
Navitas Life Sciences
Compare
Accutest Research Laboratories
Compare
Raptim Research
Compare
Perceptive
Compare
JSS Medical Research
Compare
ClinChoice
Compare
Autocal Solutions
Compare
National Environmental Engineering Research Institute
Compare
Similar Jobs for you
Clinical Research Associate - I
0-3 Yrs
Warangal, Hyderabad / Secunderabad, Nizamabad
Pharmacy, Logistics, Hospital Administration +5 more
Finance And Accounts Team Lead
2-4 Yrs
₹ 22.5 - 30L/yr
Mexico
ERP Systems
Medical Monitor
0-4 Yrs
Hyderabad / Secunderabad
SAP CO, Software Configuration Management, Clinical Research +5 more
Research Associate Medical Writing
0-3 Yrs
Hyderabad / Secunderabad
Pharmacy, Software Configuration Management, Excel +4 more
Project Manager Clinical Research
7-10 Yrs
Warangal, Hyderabad / Secunderabad, Nizamabad
Cron, Pharmacy, Clinical Research +7 more
Clinical Research Associate - II
3-8 Yrs
Warangal, Hyderabad / Secunderabad, Nizamabad
Cron, Pharmacy, Pharmacovigilance +6 more
Clinical Research Associate - III
4-9 Yrs
Warangal, Hyderabad / Secunderabad, Nizamabad
Cron, Pharmacy, Pharmacovigilance +6 more
Trainee Research Associate (C)
0-1 Yrs
Warangal, Hyderabad / Secunderabad, Nizamabad
Pharmacy, Excel, Medical Writing +3 more
Trainee Research Associate (C)
0-1 Yrs
Warangal, Hyderabad / Secunderabad, Nizamabad
Auditing, Quality Inspection, Training +3 more
Share an Interview