HCL Urgent Requirement for Healthcare Counselor(bengali/tamil/punjabi) HCL Technologies Limited

 

  

 

Job Description

Dear Candidate,
We are pleased to inform you about the opening in Noida with the No. 1 Employer in India, HCL Technologies - Business Services for the profile of Health Care Counselor (Bengali/Tamil/Punjabi).
You can come for the Direct Walk-in on 26th & 27th Oct '2015 and collect On-Spot Offer Letter based upon the selection.
Process: Health Care
Designation : Counselor
Benefits of Joining HCL BPO:
*Pickup/drop facility
*Opportunity to fast track career growth
*International Standard Facilities
*Recreation, Cafeteria, ATM and Concierge facilities
*Regular Get together and other cultural programs
*Shuttle Facility available from Noida City Metro Station
Job Description :


Shift Window: 8 am - 8 pm
Salary : Best in the industry
Scope of the Role:
* Scheduling the appointments.
* Providing the Scheduled Appointments Details.
* Handling of customer/Patient Queries.

Key Roles and Responsibilities:
* Scheduling the appointments.
* Providing the Scheduled Appointments Details.
* Handling of customer/Patient Queries.

Domain, knowledge, skills and ability:
* Biology, Medical Terminologies.
* Knowledge of Pathology Test & Medical Specialties.
* Adequate working Knowledge of MS Office.

Verbal & Written communication / Language skills :
* Excellent Communication Skills Required.
*Fluency in Bengali/Tamil/Punjabi.
#Freshers and Experienced Both Can Apply
#Cabs Available
#No night shifts
Eligibility :
Good communication Skills
Education : B. Sc / M.Sc / B.Pharm / M.Pharm / Nursing.
Venue:
HCL Technologies Limited, N5 Building,
A-22, Sector - 60, Noida", UP - 201307
Walk in timings: 11.00 am to 6.00 pm
HR Contact: Priyanka Bisht

Also write Priyanka Bisht  on top of your resume.
*All candidates should carry resume & 1 passport size photograph

Sr. Executive / Officer-drug Regulatory Affairs- Verve Health Care Ltd

Job Description

 

Preparation and compilation of dossier(s) of Finished Product in CTD and ACTD format for ROW countries.
To prepare registration dossiers for various other countries as per country specific regulatory requirements.
To prepare & submit complete & accurate registration / re-registration documents & samples well within time & to reply to queries as may be raised by registration authorities.
To co-ordinate for samples to be submitted for registration.
Documentation, Review like MFR,PVR,AMV,STPs etc..
Coordinating with different departments regarding regulatory and quality compliance practices and for documentation.
Coordinating with relevant institutions regarding conduct of Bioequivalence studies, providing them with details of the innovator product and other specific requirements of the respective countries.
Providing guidelines for developing Packaging and Labels as per Global Labeling.
Search and retrieve the different registration guidelines and to keep the same as a data bank for ready reference (Database Management)

APPLY ONLINE

Publication Support Specailist Cactus Communications

Job Description

 

What is publication support?

Under publication support, we offer a full range of services to meet authors publication needs. These services include helping authors select the most appropriate journals in which to publish their papers, preparing their manuscripts for submission, and helping them complete the journal submission process.

Would you like to help authors publish their research? And in the process learn from authors of different nationalities and widely diverse subject areas? If yes, then the CACTUS Publication Support team is the place for you! Working with us as a Reviewer will enable you to leverage your scientific knowledge in a corporate setup and engage in what you know best and are passionate about effective scientific communication.

Job Description

• Quality assurance of assignments turned in by freelance experts and providing them with constructive feedback
• Preparing and editing images and tables according to journal specifications
• Understanding client requirements and applying them to the different components of the publication support process (formatting manuscripts, checking submission requirements)
• Supporting the publication support managers in project management
• Driving or contributing to team initiatives, e.g., creation and management of resources

Location: Andheri (West), Mumbai

You fit the bill if you have:

• A Masters degree in any field of biological, physical or social sciences; candidates with a strong research orientation are preferred
• Strong command over the English language
• Strong client focus and work ethic (adherence to client requirements essential!)
• Good time management skills; strong deadline focus
• Ability to multitask across projects
• Willingness to take on the challenge of working in different subject areas

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Senior - Clinical Research Associate (vaccine)-Mumbai, Gurgaon

Job Description

Performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and PPD SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel. May assist project manager or clinical team manager on assigned projects and/or may assist in the mentoring and training of junior clinical team members.

Responsibilities:

• Monitors investigator sites to ensure the accuracy and validity of CRF entries in relation to patient records/clinic notes (source document verification). Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalate observed deficiencies and issues to clinical management expeditiously, present solutions and follow all issues through to resolution. Provides updates on potential trends noted across multiple sites and discusses potential strategies for their management to the Clinical Team Manager (CTM). Maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan.
• Participate in investigator meetings as necessary. Identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiate clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensure trial close out and retrieval of trial materials
• Manage the essential documents, as required by local regulations and ICH GCP, before, during and after a clinical trial.
• Contribute to the project team by mentoring new members, assisting in preparation of project publications/tools including informed consents, CRF guidelines and monitoring plans, and sharing ideas/suggestions with team members. Assist in project specific training for the clinical team where necessary. Identify areas for potential process improvements & share potential solutions for improvements.
• Perform additional tasks as assigned by CTM or Clinical Manager of CRAs (CM-CRA) (e.g. trip report review, newsletter creation, lead CRA team calls etc).
• Provide trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensure study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Perform QC check of reports generated from CTMS system where required.
• Facilitate effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
• Respond to company, client and federal regulatory requirements/audits.
• Maintain & complete administrative tasks such as expense reports and timesheets in a timely manner

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TCS is Hiring B. Sc Fresher for Clinical Research- Back Office Process Tata Consultancy Services Ltd.

Job Description

 

Process: Life Science - Back Office . (Only Night shift)
Experience: 0 to 3 Month experience only. (2015 pass out)
Job Location: Mumbai
Skills: Good Communication skills (Written & Verbal)


Eligibility:
. Courses considered: BSC Fresher ONLY (Chemistry / Biology/ Botany/ zoology ) 2015 passout
. Candidates who have more than 3 month experience DO NOT apply
. B.E/ B.Tech / MCA / MSc / MBA/ BMM/ BMS/ MSc/ MPharm. Strictly need NOT apply.
. Only full time courses considered.
.Should NOT have 2 years break in education.
.Should NOT have any backlogs.
.Should NOT have attended any TCS interview in last 6 months.
.Should be willing to work in NIGHT SHIFTS.(Only Night shift)


Interested Candidates are requested to forward your resume to satish.sugunan@tcs.com or what app on 7276546193.