Clinical Trial Coordinator Work from home-Apply now

About Company

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our team in clinical research services, where we bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, part of our leading global contract research organization (CRO), powers our PPD® clinical research portfolio.

Position Name :Clinical Trial Coordinator

Organization :Thermo Fisher Scientific

Qualification:B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Experience:6 months to 1 year

Salary:5.8 Lacs Per Year

Location:Work From Home

Application Link

Discover Impactful Work:

Provides administrative and technical support.
Supports audit readiness by ensuring files are reviewed according to SOP and department guidance documents.
Aids in developing the critical path for site activation within assigned projects.
May use local knowledge, organization systems, external site lists, and sponsor directives to develop and review site lists for feasibility activities.

A Day in the Life:

Perform department, internal, country, and investigator file reviews, and document findings in appropriate systems.
Ensure tasks are performed on time, within budget, and to a high-quality standard. Communicate any risks to project leads.
Provide system support (i.e., Activate & eTMF) and ensure system databases are current.
Perform administrative tasks on assigned trials, including processing documents, performing (e)TMF reviews, and distributing communications.
Support scheduling of client/internal meetings.
Review and track local regulatory documents.
Maintain vendor trackers.
Support start-up team in regulatory submissions.
Work directly with sites to obtain documents related to site selection.
Collaborate with teammates to achieve goals for assigned projects.

Keys to Success:

Education:

Relevant formal academic/vocational qualification. Bachelor’s degree preferred.

Experience:

Previous experience (6 months to 1 year) that provides the knowledge, skills, and abilities to perform the job.

Knowledge, Skills, Abilities:

Ability to work in a team or independently as required.
Flexibility to reprioritize workload to meet changing project timelines.
Understanding of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs.
Good English language and grammar skills and proficient local language skills as needed.
Proficient in MS Office (Word, Excel, and PowerPoint) and ability to master all clinical trial database systems.
Effective oral and written communication skills.
Critical judgment and decision-making skills.
Ability to accurately follow project work instructions.

Benefits:

Competitive remuneration and annual incentive plan bonus.
Healthcare and a range of employee benefits.
Career and development prospects within an innovative, forward-thinking organization.
Exciting company culture that values integrity, intensity, involvement, and innovation