Quintiles is the only fully integrated biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. Our network of 23,000 engaged professionals in 60 countries around the globe works with an unwavering commitment to patients, safety and ethics — ensuring a higher level of healthcare for people. For our biopharmaceutical customers, we help them navigate risk and seize opportunities in an environment where change is constant.
Posts:
- Clinical Research Associates, (Also apply Online) (below)
Clinical Research Associate
Job Responsibilities:
* Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
* Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
* Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
* Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), Clinical Research Specialist (CRS) and/or line manager.
* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
* Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
* May provide assistance to less experienced clinical staff.
All responsibilities are essential to job functions unless noted as non-essential (N).
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
* Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
* Good therapeutic and protocol knowledge as provided in company training
* Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a lap top computer
* Good written and verbal communication skills including good command of English language
* Good organizational and problem-solving skills
* Effective time management skills
* Ability to establish and maintain effective working relationships with coworkers, managers and clients
If not able to come for interview: APPLY ONLINE
Clinical Trials Assistant
Coordinate operations and provide support to the records or imaging center. Provide reference services to all departments and personnel and distribute incoming information for integration into systems.
Job Responsibilities:
Ensure effective security, storage, and retrieval of all proprietary and client information in accordance with established procedures. Includes usage of scanning equipment.
Conduct imaging/scanning and train on imaging/scanning processes
Provide reference services to internal clients in accordance to SOPs and by maintaining accurate charge-out systems.
Sort and classify coded material for filing. Create files according to established classification system.
Maintain log and enter metadata in database to track status and facilitate accurate retrieval of information.
Coordinate work flow through assignment of tasks and establishment of procedures.
File, maintain and process reports, collections, and validations.
Maintain logs and indexes to provide status of information and assist in the collection of data for preparation of monthly metric reports.
Assist in the training of new team members on departmental procedures.
All responsibilities are essential job functions unless noted as nonessential (N).
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Knowledge of word processing, spreadsheets, and database applications.
Excellent oral and written communication skills.
Strong organization and planning skills.
Outstanding client service skills.
Excellent interpersonal skills.
Ability to handle multiple tasks within defined timelines and significant direction.
Ability to work with others.
Ability to remain focused with regards to details.
Ability to establish and maintain effective working relationships with coworkers, managers and clients
High school diploma with 3 years experience in an office environment including 1 years’ experience in a Records Management facility; or equivalent combination of education, training and experience.
If not able to come for interview: APPLY ONLINE
WALK IN INFO
NOTE: Walk-In starts at at 9 AM and first 200 candidates will be allowed.
DATE: 14th Dec, 2013
TIME: 9.00 AM
VENUE:
Prestige Tech Park 2,
Etamin Building, 3rd Floor,
Marathahalli Outer Ring Road, Bangalore
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