Current Openings
Senior Clinical Data Manager
The Sr. CDM is responsible for managing the data management activities for multiple clinical trials. Will work closely with internal team members and vendors to ensure that assigned clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals and expectations, and budget. New Haven CT location preferred, 3 days/week.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Data Management
2 months ago days ago
Medical Science Liaison
The Medical Science Liaison will prioritize contacts with key opinion leaders (KOLs) at medical centers within specific assigned regions of the US bringing insights to Celldex and providing scientific exchange to external stakeholders.
Annually: USD 0 - 0
Full Time
Remote
Medical Science Liaison
2 months ago days ago
Senior Director, Health Economics & Outcomes
The Senior Director, Health Economics & Outcomes Research (HEOR) will proactively help design and actively implement the integrated HEOR strategies and tactics to support the clinical development and commercialization of barzolvolimab.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Real World Research
2 months ago days ago
Medical Writer/Senior Medical Writer
Medical writing to include but not limited to annual reports, Investigator's Brochures, protocols/amendments, CSRs, manuscripts, regulatory submissions that reference/summarize clinical data. Researches, writes and edits pre-clinical and/or clinical reports, summarizing data from pre-clinical and/or clinical studies.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Medical Writing
2 months ago days ago
Head, Pharmacovigilance & Risk Management, Executive Director
The Head of Pharmacovigilance and Risk Management provides strategic leadership and tactical oversight of the clinical safety department. Serves as subject matter expert for all medical and safety needs. Oversee submission for safety reports, interacts with regulatory authorities, monitors safety across all programs. Reports to the CMO.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Pharmacovigilance
2 months ago days ago