Current Openings
Senior Director, Clinical Development
The Senior Director leads clinical development activities for one or more compounds in development - The position generates clinical development strategy & plans and provides medical & scientific leadership for Celldex sponsored protocols. The Senior Director oversees study patient safety, plays key roles in data collection, data cleaning and data analysis.
Annually: USD 310000 - 340000
Full Time
On-Site/Hybrid
Clinical Development
6 months ago days ago
Vice President, Medical Affairs
Leads the company’s medical affairs strategy and execution, including launch planning, medical expert engagement and development, post-marketing clinical trials, compassionate use programs, investigator-initiated trials (IITs), publications, medical education, and medical communications (e.g., medical information, call center, etc.)
Annually: USD 380000 - 450000
Full Time
On-Site/Hybrid
Medical Affairs
6 months ago days ago
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
11 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
11 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
11 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
11 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
11 months ago days ago