Top 4 Intake specialist remote Jobs in Washington Nj

Safety Lead
Precision Medicine Group —Gladstone, NJ
- $110,700 - $166,100 a year
- Online Application
- Nursing
- 5 years
- Bachelor of Science
Safety Lead
Precision for Medicine —Gladstone, NJ
- $110,700 - $166,100 a year
- Online Application
- Nursing
- 5 years
- Bachelor of Science
Quick Apply

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Safety Lead

Precision Medicine Group -
Gladstone, NJ

Apply Now

Job Details

$110,700 - $166,100 a year

Qualifications

FDA submissions
Incident reporting compliance
Database systems
Adverse event reporting
Safety regulations
Data reporting
ICH guidelines
Bachelor's degree
Data management
Adverse drug reaction monitoring
Clinical data report preparation
Clinical trial patient safety management
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Clinical research inspection readiness
Clinical quality assurance standards
Patient safety and incident reporting systems
Internal audits
Audit support

Full Job Description

Position Summary:

Responsibilities will include but may not be limited to; project specific teleconferences/meetings(i.e. Kick off meetings, internal study specific meetings, client governance meetings) Safety budget review and approval as needed, safety management plan development, oversight of serious adverse event (SAE, SUSARS) case management from intake to regulatory reporting, and providing safety expertise in a timely manner upon request from team members, clients, and study site personnel.

Essential functions of the job include but are not limited to:

Interfacing with sponsors, vendors, and other internal team members in the area of safety/PV to assist in the design and implementation of safety collection tools, processes, and reporting systems.
Participate in the assessment and set-up of a safety database to capture SAE data.
QC of documents and safety reports when needed.
Preparation and/or review of project specific safety reporting plans and medical coding plans
Preparation and/or review of safety training materials
Review of Safety related budget tasks and activities
Develop and manage standard operating procedures and work instructions.
Serve as subject matter expert for department.
Provide ongoing training and mentorship for Safety Specialists
Participate in audits and audit preparation, kick-off meetings, and investigator meetings.
Participate in the CAPA management process.
Participate in bid defenses for existing and potential clients.
Assist departmental management with resource management.
Assist departmental management with oversight.
Serve as project manager for safety standalone projects.
Lead departmental initiatives and cross-functional development activities.
Support the generation of SAE/AESI queries and tracking including oversight in the query resolution escalation efforts.
Provide input and review of responses to regulatory agency questions with regard to safety/ pharmacovigilance activities.
Assist clients and/or other departmental staff with safety-related reviews and other services.

Qualifications:

Minimum Required:

BA/BS degree
10+ years clinical safety experience
5+ years Pharmacovigilance (PV) experience

Other Requirements:

Health care professional
Hands on experience with global safety database(s), SAE case processing, and safety reports generation
Working knowledge of MedDRA and WHODrug
Working knowledge of FDA safety regulations, ICH guidelines, and Global regulations
Demonstrated knowledge of relevant regulatory agency(s) guidelines governing both Safety reporting and processing for clinical trial environments.
Demonstrated knowledge of supporting internal audits, inspection readiness and regulatory agency(s) inspection support for clinical trials including BLA or NDA approval inspections.
Excellent communication and analytical skills (written and oral).
Excellent judgment and ability to communicate complex clinical issues in a scientifically sound and understandable way.
Ability to work in a fast-paced, innovative environment while remaining flexible, proactive, resourceful, and efficient.

Preferred:

Nursing or pharmacy degree
Industry experience in CRO or pharmaceutical company
Project management experience

#LI-KH1 #LI-Remote

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

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