Vacancy for Senior Clinical Process Associate at Quintiles

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.
Quintiles is consistently cited as the most favored contract research organization (CRO) in independent surveys of the bio pharma industry and was recently named “2009 CRO of the Year” by the prestigious SCRIP Awards.

Post : Senior Clinical Process Associate

Job Description
PURPOSE
Provide project related assistance for assigned complex project(s), sites and project teams. 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.

RESPONSIBILITIES
• Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
• Establish and maintain effective project/ site communications
• Create and maintain relevant project documents
• Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information
• Participate in document management (creation, review, maintenance, storage, as applicable)

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws,
regulations and guidelines
• Strong written and verbal communication skills including good command of English language
• Results and detail-oriented approach to work delivery and output
• Good problem solving skills
• Good planning, time management and prioritization skills
• Attention to detail and accuracy in work
• Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel
and PowerPoint
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Proven ability to work on multiple projects balancing competing priorities
• Ability to coach/ mentor junior colleagues

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Candidate Profile
• Must be computer literate.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
• Bachelor's degree in a life science-related discipline, plus at least 1.5years experience as a medical writer within a pharmaceutical environment; or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS
Extensive use of telephone and face-to-face communication requiring accurate perception of speech
Extensive use of keyboard requiring repetitive motion of fingers
Regular sitting for extended periods of time
May require occasional travel.

Additional Information:
Experience: 2 years
Location: Karnataka-Bangalore
Education: B.Pharm, B.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Senior Clinical Process
Job Code: 1710827
End Date: 21^st June, 2017