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- Clinical Trial Associate
- Clinical Trial Management
- Clinical Trial Administrator
- Clinical Trial Quality Assurance Associate
- Lead Clinical Trial Associate
- Clinical Trial Researcher
- Clinical Trial Management Associate
- Clinical Trial Payments Associate
- Senior Clinical Trial Associate
- Remote Clinical Trial Disclosure Associate
Clinical Trial Associate - Remote
Company | Atlas Search |
Address | United States |
Employment type | FULL_TIME |
Salary | |
Category | Research Services,Biotechnology Research,Pharmaceutical Manufacturing |
Expires | 2023-05-21 |
Posted at | 1 year ago |
We are currently partnered with a clinical-stage biopharmaceutical company that’s currently in need of a Clinical Trial Associate. This role is responsible for supporting day-to-day operations for the company’s clinical studies. This is a fantastic opportunity to join a company that has several assets in various stages of clinical trials for solid tumor and hematologic indications.
Responsibilities:
- Assist Clinical Project Management team in the collection, review and filing of site Essential Documents, and maintenance of the TMF.
- Develop and distribute meeting agendas, minutes and monthly status reports to document key project updates and communications to relevant stakeholders, as requested.
- Support Clinical Project Management team in communication to CRO, Vendors and Investigator Sites.
- Support the Clinical Project Management team with study start-up activities, to include preparing and/or reviewing study-related documents (e.g., Monitoring Plan, Laboratory Manual, Clinical Site Procedures Manual, Pharmacy Manual, and CRF Completion Guidelines, study logs and forms Site Contracts and Budgets, Vendor Contracts and Budgets, etc.).
- Assist in the tracking of clinical supplies at site in coordination with established systems such as IWRS, EDC and CTMS as needed.
- Support the Clinical Project Management team in the tracking of subject recruitment at all study sites; monitoring visits and approval; infringements, breaches, and misconduct, fraud, and negative trends and protocol deviations. Notify CRO and sites of updates on global study information.
- Participate in regular team meeting / teleconferences; CRO, Vendor and Investigator Site meetings as necessary; and Investigator Meetings, as necessary.
Requirements:
- Ability to travel as required.
- Minimum of 2+ years of industry experience
- Bachelor’s Degree in health science or related field
The annual base salary range is $75,000 to $90,000. Actual compensation offered to the successful candidate may vary from posted hiring range based upon geographic location, work experience, education, and/or skill level, among other things. Details about eligibility for bonus compensation (if applicable) will be finalized at the time of offer.
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