FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Assistant Clinical Research Associate / Clinical Research Associate / Senior Clinical Research Associate
AbbVieClinical Research Associate overseeing medical operations and managing study sites for AbbVie in Turkey. Contributing to high-quality clinical research within a collaborative environment.
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
GCPclinical researchproject managementdata deliverystudy site managementclinical study activitieslife sciencesbiomedical engineeringmolecular biologychemical engineering
Soft Skills
communicationtime managementcollaborationorganizational skillsstakeholder managementproblem-solvingattention to detailadaptabilityleadershipteamwork
Tools & Technologies
Microsoft WordMicrosoft ExcelMicrosoft PowerPoint
Industry Keywords
clinical study conductlife sciences degreeclinical research requirementslocal laws and regulationsmedical operationsstudy planningoversightdata qualitycross-functional collaborationindustry experience
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Responsible for managing study sites in studies overseen by Medical Operations
- Ensure that all activities are conducted in accordance with relevant processes, procedures, and applicable local laws and regulations
- Support timely and high-quality delivery of data
- Play a key part in the planning, coordination, oversight, and delivery of clinical study activities
- Work closely with the Medical Operations Manager and cross-functional stakeholders
Requirements
What you’ll need- A university degree in a life sciences discipline such as Medicine, Pharmacy, Bioengineering, Molecular Biology & Genetics, Chemical Engineering, Chemistry, Biology, or a related field
- Fluency in English
- Solid knowledge of GCP and clinical research requirements
- Strong proficiency in Microsoft Word, Excel, and PowerPoint
- Excellent project management, communication, and time management skills
- A collaborative mindset and the ability to work effectively with internal and external stakeholders
- Preferably a minimum of 2 years of industry experience in clinical study conduct
- Exposure to clinical research and participation in clinical study activities
Benefits
Comp & perks- Employee development programs
- Collaborative work environment
- Equal opportunity employer