FIND A CAREER AT
EMERGENT CLINICAL CONSULTING
JOIN THE TEAM
Emergent’s hiring process is an important part of our culture. We care about the people on our teams both personally and professionally.
We are always hiring skilled talent from entry level to leadership roles.
We’re hiring:
Position: Project Managers
Role and Responsibilities
Responsible for all management aspects of clinical trials which include sponsor teleconferences, vendor management, clinical site interaction and collaborating with the internal team in support of client deliverables. Requires flexibility, excellent interpersonal skills, previous industry experience, and the ability to work well with all levels of staff, as well as outside clients and vendors. Sensitivity to confidential matters is required.
Qualifications and Education Requirements
- 8+ years of relevant experience
- Bachelor’s Degree or higher
- Detail-oriented
- Excellent communication skills
Preferred Skills
Experience in the following areas are preferred:
- Clinical trial management
- Clinical trial technologies
- Medical Device experience a plus
Position: Project Coordinators
Role and Responsibilities
Performs project coordination duties which may include communicating with sites for essential documents, participating on sponsor teleconferences, and collaborating with the internal team in support of client deliverables. Requires strong computer and Internet research skills, flexibility, excellent interpersonal skills, project coordination experience, and the ability to work well with all levels of staff, as well as outside clients and vendors. Sensitivity to confidential matters is required.
Qualifications and Education Requirements
- 3+ years of relevant experience
- Bachelors Degree or higher
- Detail-oriented
- Excellent communication skills
Preferred Skills
Experience in the following area are preferred:
- Medical device or diagnostic trial management
- Clinical trial technologies
- MS Word
- MS Excel
- MS Powerpoint
Position: CRAs
Role and Responsibilities
Responsible for assisting with the selection, initiation, regular monitoring and closeout of investigative sites. Requires flexibility, excellent interpersonal skills, previous industry experience, and the ability to work well with all levels of staff, as well as outside clients and vendors. Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data is a must. Sensitivity to confidential matters is required.
Qualifications and Education Requirements
- 3+ years of relevant experience as Clinical Research Associate
- Experience with Medical Device and/or Diagnostics trials
- Bachelor’s Degree or higher
- Detail-oriented
- Excellent communication skills
Preferred Skills
Experience in the following areas are preferred:
- Clinical trial technologies including Electronic Data Capture