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Work as Senior Clinical Process Associate at Quintiles

 

Clinical courses

 

Clinical courses

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 : Sr. 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 
1. 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 
2. Establish and maintain effective project/ site communications 
3. Create and maintain relevant project documents 
4. Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information 
5. 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
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
- Bachelor's degree in life sciences or related field and min 2 years relevant experience; or equivalent combination of education, training and experience
PHYSICAL REQUIREMENTS
- Extensive use of keyboard requiring repetitive motion of fingers.
- Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
- Regular sitting for extended periods of time.
- May require working in shifts.

Additional Information:
Location: Maharashtra-Thane
Experience: Min. 2 yrs
Industry Type: Pharma/ Biotech/Clinical Research
End Date: 21st September 2017
Functional Area: Clinical Process

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