Top 161 Pharmacovigilance Jobs in Remote

Assoc. Medical Director (Rheumatology, Remote)
Lenox Executive Search —Remote
- $150 - $170 an hour
- Contract
- Remote
- Background check
- Medicine
- Doctoral degree
Quick Apply
Senior Director Biostatistics - REMOTE
Penfield Search Partners —Remote
- Remote
- Doctor of Philosophy
- Neurology
- Mentoring
Quick Apply
6d
Pharmacovigilance Consultant – PV Systems & Operations
EDM Pharma Consulting, LLC —Remote
- $125 - $175 an hour
- Part-time
- System design
- Databases
- Bachelor's degree
Quick Apply
2d
Adjunct Faculty - Foundations of Pharmacovigilance
MCPHS —Remote
- $2,700 - $3,000 a month
- Background check
- Mid-level
- Bachelor's degree
4d
Consultant - Pharmacovigilance/Safety Systems Implementation (Remote)
Veeva Systems —Remote
- $80,000 - $200,000 a year
- Full-time
- Remote
- Computer science
- Computer Science
- Up to 50% travel
- Paid holidays
- Health insurance
Associate Director, R&D Quality Good Pharmacovigilance Practice
BeiGene —Remote
- $143,400 - $193,400 a year
- Full-time
- Computer literacy
- Bachelor of Science
- Master's degree
- Health savings account
- Employee stock purchase plan
Senior Consultant - Pharmacovigilance/Safety Systems Implementation (Remote)
Veeva Systems —Remote
- $80,000 - $200,000 a year
- Full-time
- Remote
- Oracle
- Computer Science
- Up to 50% travel
- Paid holidays
- Health insurance
Drug Safety Pharmaceutical Consultants
Lachman Consultant Services —Remote
- Online Application
- Bachelor of Science
- Data analysis skills
- Bachelor's degree
Senior Director, Global Medical Safety, Global Pharmacovigilance (psychedelics)
Otsuka —Remote
- Full-time
- Medicine
- Office
- Travel
- AD&D insurance
- Paid holidays
Vice President, Pharmacovigilance
Vera Therapeutics, Inc. —Remote
- $300,000 - $420,000 a year
- Medicine
- BC/BE
- Continuous improvement
- Paid holidays
- Health insurance
Case Manager - Rare Disease- US Eastern Remote
Amgen —Atlanta, GA
- $81,851.60 - $110,740.40 a year
- Remote
- HIPAA
- Mid-level
- Master's degree
- Disability insurance
- Health insurance
7d
Medical Science Liaison
Corza Medical —Remote
- $150,000 - $175,000 a year
- Full-time
- Remote
- 5 years
- Surgery
- Bachelor's degree
- Continuing education credits
- Health insurance
Vice President, Drug Safety/Pharmacovigilance
Crinetics Pharmaceuticals —Remote
- $339,000 - $424,000 a year
- Full-time
- Medicine
- System design
- Laboratory experience
- Employee stock purchase plan
- Paid holidays
Business Consultant - Life Sciences R&D
Veeva Systems —Remote
- $70,000 - $140,000 a year
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
- Paid holidays
- Health insurance
Director, Pharmacovigilance Operations
Neurogene Inc. —Remote
- Nursing
- 5 years
- Writing skills
Quick Apply
1d
Medical Science Liaison
Medexus Pharma —Remote
- Medicine
- Up to 50% travel
- Doctor of Philosophy
Medical Director/Senior Medical Director, Drug Safety and Pharmacovigilance
Neumora —Watertown, MA
- $280,373 - $363,780 a year
- Remote
- Medicine
- 5 years
- Neurology
- Employee stock purchase plan
- Disability insurance
Quick Apply
Associate Director, Clinical Quality Assurance
Vera Therapeutics, Inc. —Remote
- $140,000 - $210,000 a year
- Remote
- 8 years
- Bachelor's degree
- Continuous improvement
- Paid holidays
- Health insurance
10d
Senior Clinical Programmer Contractor
Arcus Biosciences —Remote
- Contract
- Remote
- Computer Science
- Mid-level
- Master's degree
11d
Senior Labelling Strategist
High5 —Jersey City, NJ
- $50 - $58 an hour
- Temporary
- Remote
- Analysis skills
- Bachelor's degree
- Conflict management

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Assoc. Medical Director (Rheumatology, Remote)

Lenox Executive Search
Remote

Quick Apply

Job Details

Contract
$150 - $170 an hour

Qualifications

Doctoral degree
Biostatistics
Rheumatology
ICH guidelines
Clinical staff training
Data management
Clinical training
Clinical staff mentoring
Team training
Clinical quality assurance standards
Patient safety and incident reporting systems
Staff development

Full Job Description

12+ month extendable Remote CONTRACT role. Must be able to work EST hours, 7:00AM-4:00PM M-F. Must be MD board certified in Rheumatology. Previous Pharma industry experience highly preferred. Pay rate $150-$170/hour depending upon experience.

Lenox Executive Search is seeking an experienced Assoc. Medical Director to fill an 12+ month extendable contractual role with a global pharmaceutical company. Must have therapeutic expertise in Rheumatology.

REQUIREMENTS for the Assoc. Medical Director:

MD board certified in Rheumatology - MUST HAVE
Candidates should have at least one of the following: Clinical experience in treating patients in the speciality or sub-speciality associated with the applicants training (comparable to 2 years); Or Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or direct experience in safety/Pharmacovigilance (comparable to 2 years)
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Therapeutic expertise in Rheumatology
Working knowledge of relevant safety databases (e.g. Medra)
Flexibility to travel domestically and internationally (10% of time)
Understanding guidelines (FDA, ICH, EMA and GCP)
Working knowledge of biostatistics, data management, and clinical operations procedures
Ability to act as a mentor/trainer to other staff
Must be able to work EST hours (M-F, 7:00AM-4:00PM)

RESPONSIBILITES of the Assoc. Medical Director:

Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed.
Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities.
Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g. labeling reconciliation documents, CTD modules, REMS, RMP and CSR).
Manages all medical aspects of contracted tasks across the pharmaceutical product life-cycle.
Ensures tasks delegated to PVG are properly executed. Adheres to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Adheres to client SOPs/directives and project specific WPDs for assigned projects. Adheres to PPD’s corporate policies and SOPs/WPDs.
Provides medical consultation to team members and answer all study related medical questions. Communicates clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately.
Provides therapeutic training and protocol training on assigned studies, as requested.
Assists in writing (interpretation of safety and efficacy data) and/or review of CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc. to ensure that the medical content is accurate and complete.
Monitors all safety variables (AE, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medication for protocol restrictions, and un-blinding requests) of clinical studies
Discusses all medical concerns with principal investigators and clients (e.g. discussion regarding interpretation of inclusion/exclusion criteria) raised during the course of a study, using proper medical judgment in the interpretation and decision making with regard to clinical situations as they relate to the investigational study.
Provides medical review of adverse events of special interest, serious adverse events and clinical outcomes events reported by study sites.
Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess for potential safety concerns.
Manages signal detection activities, scientifically reviews aggregate reports, contributes to label updates, supports dossier maintenance and risk management activities.
Medically reviews adverse event and serious adverse event data from all sources (solicited, spontaneous, literature, etc) as contracted.

Pay: $150.00 - $170.00 per hour

Application Question(s):

Able to work EST hours

Education:

Doctorate (Required)

Experience:

therapeutic Rheumatology: 2 years (Required)

License/Certification:

Board Certification in Rheumatology (Required)

Work Location: Remote

Quick Apply

Refine Your Search

pharmacovigilance jobs in remote

Assoc. Medical Director (Rheumatology, Remote)

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