Clinical Trial Coordinator Level I or II (Client dedicated)
Our global Clinical Operations colleagues within our PPD clinical research services provide
-
- end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute
- quality,
- efficient clinical studies.
Position Overview:
Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document. Provides administrative support for site activation activities. Aids the development of the critical path for site activation within assigned projects in support of rapid site activations. Represents CRG personnel. May apply local knowledge, organization systems, external site lists and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. Might be assigned as a buddy during onboarding phase and provide training to new staff as needed.
Essential Functions:
- quality standard. Proactively communicates any risks to project leads.
TMF) and ensures system databases are always current.
- clinical study supplies to sites.
- specific translation materials and translation QC upon request.
- site feasibility visits (Asia Pac only).
TMF). May support RBM activities.
- up team in Regulatory submissions.
- tup activities within the site activation critical path are aligned.
- out of global strategic feasibility processes and standard methodologies.
Keys to Success:
Education and Experience:
High/Secondary school diploma or equivalent and relevant formal academic / vocational qualification. Bachelor's degree preferred. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities
- specific data/systems to ensure accuracy and efficiency
- clinical/clinical aspects of project implementation, execution and closeout
Point) and ability to obtain knowledge and master all clinical trial database systems
- making skills
Why Join Us?
We hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore you will benefit from an , ensuring you reach your potential.
What We Offer:
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and
- being of our employees. We have a , where PPD clinical research services truly value a
- life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.
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