POSITION CLOSED: Vasta Bio- Informatics Pvt. Ltd (Mumbai): Clinical Research Co-ordinator | CTC Upto: 4.44 lacs P.A | JC/1939

Dear Team,

 

Thank you for your support.

 

Please do not source any more profiles as we has successfully closed.

 

As always, appreciate your support.

 

-------------------------------------------------------------------------------

 Dear Team,

 

Please work on the below requirement. Request you to kindly share suitable resumes.

 

Interview Process:

·         Post CV Screening Akshara will provide a time slot to connect your candidate for a con call

·         Post her short listing, candidate’s profile will be shared with the client

·        Immediate joiner or 30 days notice period and buy out option is available

·        Work from office

·        Feedback TAT- 4 days

 

Role	Sourcing Date	Candidate name	Mobile#	Current / last designation	Experience (years)	Current salary	Expected salary	Notice period	Qualification	Reason for change	Current Location

 

About us (VASTA BIOINFORMATICS PVT Ltd. – VBPL):

 

Vasta is headquartered in New York, USA committed to provide sustainable and scalable solutions for your clinical research and bioinformatics needs. Their team has almost a decade worth of experience in medical information management especially cancer research. Good data drives quality research.

They recognize that today’s research will shape the clinical practice guidelines of tomorrow. Their information technology and data management solutions can streamline and integrate research and patient care workflows to collect quality data and achieve research goals.

 

Company Website:

 

https://www.vastaglobal.com/

 

Reporting To: Project Manager

 

Job Code	JC/1939
Process	Operations & Delivery
No. of Requirements	2
Gender	Male/female
About Process	Responsible for the management of designated clinical trials, preparation of trial related documentation per protocol and Case report forms (CRF)
	Ensure completeness and submission of data into the data collection form (e.g., electronic CRFs, cancer research database (CRDB), PC-based systems, remote data entry) as per protocol requirements and time lines
	Tracking completed CRFs and setting up systems whereby completed CRFs are rapidly entered into the database. Ensure that queries generated during cleaning are responded to in a timely fashion and in compliance with ICH-GCP guidelines
	Ensure the conduct of the trial is in compliance with the currently approved protocol/amendment
	To significantly improve quality assurance and consistency in electronic data capturing and data
	Participate in global conference calls and meetings to review progress of ongoing clinical trials
	Verify that the investigator followed the approved protocol and all GCP procedures
	Communicate any observations to the sponsor i.e. deviations/violations to protocol, safety alerts, quality issues, etc. that may affect the quality of the protocol
	Complete regulatory requirements, as applicable
Title	Clinical Research Co-ordinator
Location	Turbey,Navi Mumbai
Requirement	Minimum 1 - 2 years of experience in Clinical Trials Management/Protocols
	Excellent communication skills – written and verbal
	Proficient in the knowledge of protocol monitoring activities
	Knowledge of Oncology Specific terminology preferred
	Knowledge of EDCs such as Medidata RAVE, Oracle, Inform, etc. strongly preferred
	Experience with Industrial protocols and monitoring visits strongly preferred
	Hands-on with computer skills
	Ability to multitask, work under pressure and meet deadlines required
Education	Bachelors/ Masters Degree
Shift timings	9:30am - 5:30pm
Transport Boundaries	Candidates who can travel till work location
Transport Facility	Available
Salary Range	UG: 20,000 P.M - 22,000 P.M | PG: 22,001 P.M - 24,000 P.M - EXP 0 - 1 year
	UG: 29,001 P.M - 34,000 P.M | PG: 32,001 P.M - 37,000 P.M - EXP 1.1 years - 2 years
Weekly Off	Saturday and Sunday fixed off
Age	Upto 40 years
USP	Brand, salary, designation, shift and transportation facility
Rounds of Interview	HR
	Technical
Documents	Educational + Identity Proof + Residential Proof + Offer Letter + Salary Proof (Bank Statement/Payslip) + Relieving Letter
Claw back	90 days