Novartis Pharma Associate Job Vacancy - Clinical Research

Novartis Pharma Associate Job Vacancy – Clinical Research

Novartis MPharma Job M.Pharma Associate job openings. Pharmaceutical Jobs. Applications are invited for the post of Associate @ Novartis. Career @ Novartis Pharma job opening .vacancy at Novartis. Interested candidates may apply online. Novartis Pharma jobs 2019. Check out all the details and apply online.

Job ID 279853BR

Position Title Senior Clinical Research Associate

Eligibility Criteria:

  • Degree in scientific of healthcare discipline. Master degree preferred Fluent English (oral and written).
  • Ideally 4+ years of pharmaceutical industry experience with 3 years of strong experience in clinical research
  •  Experience in a monitor role or a role overseeing clinical trials
  • Strong interpersonal skills
  • Strong Project Management and leadership skills
  • Working experience in a global team, team player
  • Ability to work in a matrix environment
  • Displays innovative ideas and solutions
  • Highly proficient in negotiation skills

Job Description
Your responsibilities:
Your responsibilities include, but are not limited to:

1. Nominate new sites for clinical trials; analyze capability and make a recommendation for trial inclusion
2. Assume ambassadorial role to facilitate communication between sites and Novartis line functions and increase value proposition to investigators
3. Facilitate the preparation and collection of site-level documents; resolve problems as required
4

. Execute site initiation and training
5. Implement total site management including monitoring visits, regulatory assessment, drug supply management and resolution of site problems to ensure compliance
6. Track trial execution milestones; identify problems; resolve issues and escalate as appropriate 7. Manage recruitment and execute contingency plans, as needed
8. Complete preparation/generation of study monitoring reports
9. Manage data at the site; resolve technical and content issues to achieve aggressive database lock targets
10. Implement site closeout activities across all sites and performs SCV for own sites in a timely manner
11. Act as local and/or global CRA lead, author global monitoring plan and Local SOPs as assigned
12. Act as a mentor to new associates for purposes of field training, as assigned
13. Participate in multi-disciplinary teams within CPO and globally to evaluate and implement process improvement
14. May be involved with special projects and workstreams 1
5. Mentor new associates

Apply Online

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