Johnson & Johnson

Manager, Safety Analysis Scientist

Johnson & Johnson • $117K — $201K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in healthcare-related or biomedical science with 9+ years of industry experience or equivalent.
  • Advanced degree preferred with 6+ years of industry experience or equivalent.
  • Medical writing or pharmacovigilance experience required.
  • Clinical experience preferred, enhancing practical application of safety evaluations.
  • Strong understanding of medical concepts in drug development and safety requirements needed.

Responsibilities

  • Lead safety evaluations and oversee strategy discussions with cross-functional teams.
  • Ensure high-quality safety reports with minimal revisions needed.
  • Support novel projects by guiding associates in undefined processes.
  • Review key regulatory and clinical documents to ensure compliance.
  • Demonstrate leadership within Safety Management Teams and assist the Medical Safety Officer.
  • Prepare and present safety data, maintaining accurate meeting records.
  • Conduct proactive reviews of safety data to assess emerging risks.

Benefits

  • 120 hours vacation per calendar year.
  • 40 hours sick time, varying by location.
  • 13 days paid holidays per year, including floating holidays.
  • Up to 40 hours work, personal, and family time off each year.
  • 480 hours parental leave within one year of a child's birth or adoption.
Full Job Description
Job Function:
Product Safety

Job Sub Function:
Product Safety Risk Management

Job Category:
Scientific/Technology

All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, United States of America

Job Description:

We are searching for the best talent for our Manager, Safety Analysis Scientist to be located in Horsham, PA; Titusville, NJ; or Raritan, NJ.

Purpose: The Manager, Safety Analysis Scientist (SAS) provides scientific expertise for the safety assessment of assigned products, partnering with the Medical Safety Officer (MSO) to support regulatory compliance and safety-related decision-making for marketed and in-development products.

With in-depth product knowledge, the Manager SAS serves as the product point of contact and mentors team members on complex reports. The role operates independently or with moderate guidance from the Director, SAS Therapeutic Area Lead (TAL), building the cross-functional alliances needed to shape safety-related decisions and outcomes.

You will be responsible for:

  • Leading safety evaluations, including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)/MSO and other team members as necessary, data retrieval, data analysis, report writing, and report revision.
  • Ensuring high quality safety evaluations and reports with minimal-to-moderate comments from team members and minimal-to-moderate revisions required.
  • Providing support to AD SASs for novel projects without defined processes.
  • Providing input and review to key regulatory or clinical documents as appropriate.
  • Demonstrating leadership in the SMT and support the MSO.
  • Supporting SMT activities (e.g. preparing and presenting data, compiling meeting minutes, updating signal tracking information).
  • Leading proactive safety data reviews.

Qualifications/Requirements

  • Bachelor's Degree Required: Healthcare-related or Biomedical Science (9+ years industry experience or equivalent).
  • Advanced Degree Preferred: Healthcare-related or Biomedical Science (6+ years industry experience or equivalent).
  • Medical writing or PV experience required.
  • Clinical experience preferred.
  • Working knowledge of medical concepts and familiarity with safety activities in drug development and post marketing and global safety health authority requirements is required.
  • Ability to understand and analyze complex medical-scientific data from a broad range of sources is required.
  • Ability to interpret and present complex data to determine benefit-risk impact is required.
  • Excellent English verbal and written communication skills is required.
  • Ability to effectively interact with team members, including business partners is required.
  • Ability to work in a cross-functional team environment, proven leadership skills is required.
  • Ability to plan work to meet timelines and effectively balance multiple priorities is required.
  • Proficiency in Microsoft applications (e.g. Word, Excel, and PowerPoint) is required.
  • Ability to influence, negotiate and connect with both internal and external customers is required.


#LI-Hybrid

Required Skills:

Preferred Skills:
Business Alignment, Clinical Operations, Coaching, Compliance Management, Compliance Risk, Critical Thinking, Data Reporting, Medicines and Device Development and Regulation, Organizing, Quality Control (QC), Research Ethics, Researching, Risk Management, Safety Investigations, Safety-Oriented, Serious Adverse Event Reporting, Standard Operating Procedure (SOP), Technical Writing

The anticipated base pay range for this position is :
$117,000.00 - $201,250.00

Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation -120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year

Holiday pay, including Floating Holidays -13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave - 80 hours in a 52-week rolling period10 days

Volunteer Leave - 32 hours per calendar year

Military Spouse Time-Off - 80 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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