Quintiles Walk-in Event on 28-nov-15 (clinical Research Professionals) Quintiles 1 - 6 yrs Bengaluru/Bangalore

Greetings from Quintiles!

We are having a walk in event for the below roles:

1. ClinicalResearch Professionals Candidates with 1 to 8 years of experience in clinicalresearch field. Preferably candidates with site monitoring experience. (Job # 1517352)

2. Project Management professionals candidates with 5+ years of experience in line management in clinical / healthcare

domain (Job # 1517361)

3. ClinicalResearch freshers looking for candidates with strong clinical background and communication skills who have good domain knowledge (Job # 1524797)

All roles require excellent communication skills and will involve working in shifts.

Interview Location:

Quintiles
Etamin Block, Wing A, Ground floor
Prestige Tech Park II, Outer Ring Road
Sarjapur, Bangalore - 560103


Clinical Roles:

PURPOSE

Apply clinicalresearch expertise to provide project related assistance across complex and multiple project(s), sites and project teams. Lead teams functionally, where assigned, including awareness of scope of work, budget, and resources. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.


REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Advanced knowledge of clinical trial conduct, and skill in applying applicable clinicalresearch regulatory requirements;

i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Familiarity with related systems and software utilized in clinical operations.

Strong written and verbal communication skills including good command of English language

Results and detail-oriented approach to work delivery and output

Project Control Professionals:

The Project Controls Professional (PCP) assists in the monitoring, controlling and communication of project performance. This position reports to the Clinical Project Manager, through a dotted line reporting relationship, and is responsible for directing and/or coordinating project planning & scheduling, estimating, cost control, change management and risk management.

Roles & Responsibilities:

General Attributes

1. Establishes and maintains a project monitoring, control and reporting system that supports on-going assessment of project performance and facilitates informed and timely adjustment of project execution to achieve project objectives

2. Develops and maintains the Project Execution Plan sections related to project tracking, trending, reporting and change control elements

Applies strong time management, planning, organizational, decision making and problem solving skills to resolve issues in an effective and timely matter

Interested Candidates Please forward your resume to sindoora.kn@quintiles.com or directly Walk-in to the Venue.

Regards,
Sindoora

Openings for Freshers- Pharmacovigilance Quintiles 0 - 0 yrs Bengaluru/Bangalore

Looking for freshers who has completed their graduation B.Pharma/M.Pharma/ BDS/ M.Sc/B.Tech.

RESPONSIBILITIES
Provide intake and tracking of initial safety and clinical event validation and adjudication (CEVA) data. Transfer incoming safety/CEVA data to project team. Identify any problems with incoming faxes and bring them to the attention of the senior team member.
Distribute safety data to marketing authorization holders, customers, regulators and investigators.
Specific project responsibilities include set-up and/or maintenance of safety/CEVA files for reported events; archiving of files when closed; coordination of transfer of archived material to company/customer archive storage facilities; preparation and assistance in setting-up and updating project files; maintenance of personal safety files for mail merges and regulatory documents; where required, data entry of events into tracking database and assistance of transfer of events to customers.
Provide administrative support for the department by coordinating team/department/customer meetings, coordinating stationery orders, dispatching data via courier services, reserving meeting rooms and IT equipment; and providing secretarial support as required.
Generate and distribute alert letters.
Identify and record quality problems and bring them to the attention of a senior team member.
Provide training/mentoring new/less experienced staff.
Assist project lead and CEVA management with specific aspects of CEVA processes.
Set up and maintain Serious Adverse Event (SAE) files for reported events; organize and send files for archive when events are closed.
Coordinate, schedule and submit reports to regulatory authorities in accordance with deadlines.
Coordinate distribution of safety letters to study investigators and Clinical Research Associates.
Assist in processing incoming and outgoing Adverse Event (AE) reports by collecting and tracking incoming AE reports sent via fax, email, eCRF, etc; determining initial/update status of incoming events; tracking timelines for completion of AE processing; performing data entry into safety database; routing report information to appropriate PhV project personnel in the workflow for continued processing; performing quality control activities as directed by project lead or manager; generating established safety data reports; submitting AE reports to client and other project team members identified by project lead; obtaining confirmation of report receipt and track submission; and assuming workflow responsibilities for local and global projects.
Perform records management tasks such as creating and tracking case folders for AE reports; filing, retrieving and delivering case folders; assisting in maintenance of document control room and relevant applications/systems as directed by manager; archiving case folders and project files; assisting in creation of PhV records management processes and procedures; providing key input to management on acquisition and/or upgrade of records management application/systems; and serving as liaison between Pharmacovigilance department and records management department.

APPLY ONLINE

Open Walkin for Pharmacovigilance Experienced(2+ in pv) on 28th Nov Quintiles 2 - 7 yrs Bengaluru/Bangalore

Dear Candidate,

Open walk in for experienced(2+ years in PV) on 28th Nov 2015.

Event details:

Date- 28-Nov-2015
Registration Timings - 8 am to 9:30 am
Documents to carry Copy of this mail, Updated CV, Id proof (For experienced candidates :: last 3 months pay slip, latest compensation break up letter)
Assessment process - CV screening->Aptitude->HR Interview->Technical interview->Final interview
Job location - Bangalore
# of openings - Multiple.
Contact person Kavya L / A Shamshuddin

Interview Location
Quintiles
Etamin Block, Wing B, Ground floor
Prestige Tech Park II, Outer Ring Road
Sarjapur, Bangalore - 560103