Lanka Praneeth

Email Id: lankapraneeth@gmail.comMobile: 9032921305

Career Objective:

To secure a challenging position, to be flexible at work where my skills and knowledge are updated for achieving the organizational goals.

PROFESSIONAL EXPERIENCE :

Worked as a Site Services Specialist at ICON Clinical Research India Pvt.Ltd, Bangalore, India from 2012 September to 2015 April ( 2 years 7 months) .

Global Site Support service to Respond to Investigator Sites: To track and follow up on data updation by using one globally accessible site management database.

As Site Service Specialist I :-

Discrepancy Management: Investigate problems related to subject visits and arrive at effective resolution.

Query Management: Issue Data Queries (Data Clarification Form) and ad-dressing incoming queries/answer from sites as well as respond to internal queries until resolution is complete.

Data Entry: Data Entry of subject demographics, Subject Fasting status, & visit information.

Data Reconciliation: External Data Reconciliation as per Project Manager’s request.

Report Generation: Container / chronology management reports, Metrics and Tracking.

Database Locking: Locking activities for visits which has discrepancy. Quality review: Performing the quality on a monthly basis. Proactive Reporting: Escalate problems to the attention of the Team Lead

or Line Manager or Project Manager with the best of the available solutions. SOP: Understand and comply with core operating procedures and working in-

structions. Team Player: Develop and maintain good communications and working rela-

tionships with the sites helping each other by sharing there Knowledge. Mentoring: Assist in training of newly hired members of the team. Miscellaneous: Any other relevant task assigned by Team Lead & Project

Manager. Global sample tracking calendar controlling. Accountability of every samples received at ICON .

CRC: Worked as Clinical research Coordinator(2011 Mar to 2012 September)(7months )

At Dr.Sudhavani (Ameerpet ,Hyderabad) skin specialist

Making accountability to all the materials at the study site (Including Study Drug accountability.

Arranging the study visit of subjects to site. Maintaing Good Clinical Practice at the site.

Updating the study Documents with all the lab values ( Maintaining GDP at Site)

Trainee CRA : Worked as Trainee Clinical research Associate at Asian Clinical Trials. 2011 Jan to 2012 September) 9 months

Preparing the Minutes of Meeting. Preparing the Study documents. Preparing the presentation for the site Initiation. Identifying the potential sites and taking the agreement with the site persons. Checking the proper dispatch of the study drug to the site. Assisting the CRA in the ( Monitoring, Proper communication between the CRC

and the CRA)

Achievements:-

Recognized as the Best clinical research coordinator by the sponsor(Glen mark). Recognized as the best trainee CRA by Asian Clinical Trials. Worked as clinical data manger in the project work in Crema and made my team

stand first in completing all the tasks in the given schedule by preparing a well planned Datamangement Plan and tasks assigned to members by recognizing there Strength and Interest.

Summary :-

I had a total of 2 years 7 months as site service specialist & 1 year 5 months as Traniee CRA & CRC in Asian Clinical Trails & Sudhavani ( A total of 4 years in clinical Research )

Personal Strengths:

Curiosity to learn

Quick Learner

Good Team Player

Adaptability to Situation

 Education Qualification:

Post Graduation in Biotechnology from GITAMS University. Advanced Post Graduation Diploma in Clinical Research and Management. B-sc in life science with biotechnology, zoology, chemistry in distinction. Post Graduation diploma in Lab technician course with first class.

Computer skills:

Good knowledge in Ms office . Hands on Experience with ICOLIMS, PACS, FLEX ( Used In ICON) Lab data

management Soft wares . Theoretical knowledge of RAVE and Inform

Technical Skills:

MS office suite Developed Protocol, Investigator brochure, Budget drafts as a part of group

activity,DMP ( Data Management Plan ) Good in handling instruments like Autoclave. Centrifuge, U.V chamber , Neubauer

counting chamber. Good Knowledge about Regulatory in Clinical Research ,21 CFR Part 11. Updating Global Sample Tracking Calendar

Non – clinical Research Experience :-

From April 2015 working In EZONE as Administrator .

Some of the roles are managing the Queries ,Solving the IT related problems

Personal Profile:

Name : Lanka Praneeth

Gender : Male

Date of Birth :  28 Sep 1988

CTC : 3.41 lakhs

Languages Known :  English, Hindi and Telugu

Address : 2-86,Subhas Chandra Colony ,Enikepadu ,Krishna District

Vijayawada 521108

REFERENCES:

1. Geetha MohandasManager – Client ServicesIcon Clinical ResearchEmail: Geetha.Mohandas@iconplc.com

2. Mohammad RizwanTeam LeaderIcon Clinical ResearchMohammed.Rizwan@iconplc.com

4. Dr .SudhavaniPrincipal Investigator SKIN CARE CLINIC

Declaration

I hereby declare that the information provided above is true to the best of my knowledge.

Place:

Date: (L.Praneeth)