Top 616 Assoc Director Jobs

Assoc. Medical Director (Rheumatology, Remote)
Lenox Executive Search —Remote
- $150 - $170 an hour
- Contract
- Remote
- Background check
- Medicine
- Doctoral degree
Quick Apply
Pri Sci/Sr Pri Sci/Assoc Director - In Vivo Pharmacology
Think Bioscience —Boulder, CO
- $120,000 - $180,000 a year
- Full-time
- 5 years
- Doctor of Philosophy
- Team management
Quick Apply
Assoc Director, Biostatistics
Gilead Sciences —Parsippany-Troy Hills, NJ
- $195,670 - $253,220 a year
- Full-time
- 6 years
- Bachelor of Science
- Bachelor's degree
- Health insurance
- Dental insurance
Assoc.Managed Care Liaison Director – Southeast
Neurocrine Bioscience —Remote
- $206,400 - $282,000 a year
- Full-time
- Psychiatry
- Analysis skills
- Doctor of Philosophy
- Paid holidays
- Health insurance
Assoc Director, Statistical Programming
Gilead Sciences —Raleigh, NC
- $177,905 - $230,230 a year
- Full-time
- 5 years
- Bachelor of Science
- Analysis skills
- Health insurance
- Dental insurance
4d
Assoc. Director, Patient Support Programs
TG Therapeutics —Remote
- Email
- Remote
- 5 years
- Bachelor's degree
- Neurology
13d
Assoc Director, Real-World Evidence
Kite Pharma —Foster City, CA
- $195,670 - $253,220 a year
- Full-time
- Medicine
- Office
- Bachelor's degree
- Health insurance
- Dental insurance
Sr Manager/Assoc Director, CMC Regulatory Affairs
Erasca —South San Francisco, CA
- $175,000 - $205,000 a year
- Remote
- 5 years
- Bachelor's degree
- Quality control
- Health savings account
- AD&D insurance
7d
Assoc. Director, Research Administration (Pre-Award)
University of Miami —Coral Gables, FL
- Full-time
- Master's degree
- University
- Bachelor's degree
Assoc. Director, Athletic Equipment Operations
University of Miami —Coral Gables, FL
- Full-time
- Management
- Computer literacy
- 3 years
Senior Principal Scientist / Assoc Director, Oncology Translational Research
Novartis —Cambridge, MA
- $138,600 - $257,400 a year
- Full-time
- 5 years
- Analysis skills
- Doctor of Philosophy
- Health insurance
- 401(k) matching
Assoc Director/Director, Pharmaceutical Development
Erasca —South San Francisco, CA
- $200,000 - $225,000 a year
- Management
- Travel
- Experience equivalent to degree accepted
- Health savings account
- AD&D insurance
Assoc Director, Clinical Operations-Early Phase
Gilead Sciences —Foster City, CA
- $195,670 - $253,220 a year
- Full-time
- 8 years
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Dental insurance
Assoc Director, IT Architecture
Gilead Sciences —Foster City, CA
- $195,670 - $253,220 a year
- Full-time
- Computer Science
- HIPAA
- Research
- Health insurance
- Dental insurance
Assoc. Director of Development Communications
The Taft School —Watertown, CT
- Full-time
- School experience
- Marketing
- 3 years
Assoc. Director, Field Operations
Neurocrine Bioscience —San Diego, CA
- $171,800 - $235,000 a year
- Full-time
- Microsoft Excel
- Psychiatry
- Marketing
- Paid holidays
- Health insurance
Associate Director, Patient Engagement GDNF
Asklepios BioPharmaceutical —Remote
- Full-time
- 8 years
- Bachelor's degree
- Travel
Assoc. Dir. or Director, Clinical Project Management (remote US)
ARAVAS INC —Pennsylvania
- $145,000 - $185,000 a year
- Full-time
- Remote
- 5 years
- Bachelor of Science
- Administrative experience
- Paid parental leave
- AD&D insurance
Quick Apply
11d
Adv Energy Assoc Director
TRC Companies, Inc. —Melville, NY
- $75,649.60 - $167,000.00 a year
- Full-time
- 5 years
- Office
- Residential
- Paid holidays
- Disability insurance
10d
Operations Assoc Director
Zimmer Biomet —Baltimore, MD
- $144,000 - $181,000 a year
- Full-time
- 6 years
- HIPAA
- High school diploma or GED
- Wellness program

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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

Assoc Director jobs

Assoc. Medical Director (Rheumatology, Remote)

Pri Sci/Sr Pri Sci/Assoc Director - In Vivo Pharmacology

Assoc Director, Biostatistics

Assoc.Managed Care Liaison Director – Southeast

Assoc Director, Statistical Programming

Assoc. Director, Patient Support Programs

Assoc Director, Real-World Evidence

Sr Manager/Assoc Director, CMC Regulatory Affairs

Assoc. Director, Research Administration (Pre-Award)

Assoc. Director, Athletic Equipment Operations

Senior Principal Scientist / Assoc Director, Oncology Translational Research

Assoc Director/Director, Pharmaceutical Development

Assoc Director, Clinical Operations-Early Phase

Assoc Director, IT Architecture

Assoc. Director of Development Communications

Assoc. Director, Field Operations

Associate Director, Patient Engagement GDNF

Assoc. Dir. or Director, Clinical Project Management (remote US)

Adv Energy Assoc Director

Operations Assoc Director

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