Full-Time Medical Director
Allucent is hiring a remote Full-Time Medical Director. The career level for this job opening is Experienced and is accepting USA based applicants remotely. Read complete job description before applying.
This job was posted 2 months ago and is likely no
longer active. We encourage you to explore more recent opportunities on our site. However, you
may still try your luck using 'Apply Now' link below. We recommend focusing on newer listings
available here.
Allucent
Job Title
Medical Director
Posted
Career Level
Full-Time
Career Level
Experienced
Locations Accepted
USA
Share
Job Details
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials.
We are looking for a Medical Director to join our A-team (remote). The Medical Director works independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent.
Key tasks:
- Provide medical monitor support to assigned clinical trials.
- Assist with protocol interpretation and medical review of data.
- Provide input on Protocol design and Strategic clinical recommendations.
- Prepare Medical Monitoring and other relevant plans for assigned trials.
- Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events.
- Assist clinical data management with MedDRA and WHO coding.
- Review clinical trial documents for medical consistency and relevance.
- Assist in the set up and conduct of Data Safety Boards (DSMB, DMB or similar) and Dose escalation meetings (DEC).
- Attend and participate in Kick-Off, Investigators’ meeting, and other relevant meetings.
- Provide 24/7 urgent medical support for medical and safety advice if required.
- Training of project teams on medical aspects of the trial and therapeutic training as required.
- Support protocol deviation guidance development and review of Protocol Deviations.
- Identify trial risks and provide input to the Risk plan.
- Ensure conduct of safety reviews to identify data issues.
- Independently review and understand trial medical deliverables.
- Draft and contribute as Subject Matter Expert (SME) in the field of Medical Monitor activities.
- Assure good communication and relationships with (future) clients.
- Support Business Development efforts.
- May advise and assist clients on product development, trial designs, endpoint analyses and the feasibility of conducting Phase I to IV clinical trials.
- May provide therapeutic consultation in support of the scientific, medical, and regulatory operations of the company.
- Support in preparation of new proposals.
- Contribute and take part in client evaluations, visits and bid defense.
- Contribute to other areas of business as required.
FAQs
What is the last date for applying to the job?
The deadline to apply for Full-Time Medical Director at Allucent is
27th of October 2025
. We consider jobs older than one month to have expired.
Which countries are accepted for this remote job?
This job accepts [
USA
] applicants. .
Related Jobs You May Like
Regional Project Lead
Remote, US
2 days ago
Clinical Research
Communication
Project Management
PSI CRO
Full-Time
Manager
Clinical Trials Proposal Manager
Madrid, Spain
2 days ago
Budgeting
Clinical Trial Knowledge
Proposal Management
PSI CRO
Full-Time
Manager
Senior CRA I
Toronto, Canada
1 week ago
Clinical Study Management
Communication
CRF Review
PSI CRO
Full-Time
Experienced
Clinical Research Associate II
Saint-Maur-des-Fossés, France
1 week ago
Clinical Monitoring
Communication
CRF Review
PSI CRO
Full-Time
Experienced
Grants Expense Coordinator
Oxford, United Kingdom
1 week ago
Budgeting
Communication
Data Analysis
PSI CRO
Full-Time
Entry Level
Clinical Operations Manager
Belgrade, Serbia
1 week ago
Budget Management
Clinical Trial Management
Communication Skills
PSI CRO
Full-Time
Manager
Clinical Trials Business Development Representative
Tbilisi, Georgia
1 week ago
Business Development
Clinical Trial Knowledge
Communication Skills
PSI CRO
Full-Time
Experienced
Scientific Affairs Liaison
Lancaster, PA
2 weeks ago
Analytical Skills
Clinical Protocols
Communication Skills
Eurofins
Full-Time
Experienced
Site Contract Specialist I
Remote, Canada
2 weeks ago
Budget Management
Clinical Research
Contract Management
PSI CRO
Full-Time
Entry Level
Site Contract Specialist I
Remote, REMOTE
2 weeks ago
Budget Management
Clinical Trial Knowledge
Contract Negotiation
PSI CRO
Full-Time
Entry Level
Business Development Director (CRO)
San Diego, CA
2 weeks ago
Account Management
Business Development
Client Relationship
Ergomed
Full-Time
Manager
Clinical Trials Proposal Manager
Oxford, United Kingdom
3 weeks ago
Budgeting
Clinical Trial Knowledge
Proposal Management
PSI CRO
Full-Time
Manager