Senior Scientist, Clinical Sciences Early Development (Hematology)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

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Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at are searching for a Senior Scientist Clinical Sciences Early Development (Hematology) to be located in Spring House PA office. A pre-identified candidate has been identified however all applications will be considered.

The Senior Scientist Clinical Sciences Early Development (Hematology) works in the Oncology Therapeutic Area Development group and participates in the development oversight and execution of Ph I-IV clinical research trials working closely with Study Responsible Physicians and other Clinical Project Scientists. The position reports to a more senior Clinical Project Scientist and has the following essential job functions:

Essential Functions:

• Forongoing clinical trials this individual in collaboration with the Study Responsible Physician/other Clinical Project Scientists will participate in or lead aspects of aggregate and participant level data including patient screening/eligibility evaluation PK/PD data adverse events efficacy coding and other data critical to study endpoints

• May participate in drafting protocol synopses sections of full protocols informed consent documents and will review Case Report Forms (CRFs) and other data collection tools against draft protocols and central vendor scope of work

• May partner with the lead CPS/Cross Functional Trial Team to mitigate issues in initiation of clinical trials and may participate in review of Monitoring Guidelines SET/IDMC Charter Statistical Analysis Plan Data Management and Safety Management Plans

• May liaise with vendor laboratories Translational Research lead pharmacokinetic operations and/or biomarker operations to ensure sample collection processing and tracking

• May liaise with Integrated Data Analysis & Reporting team in set-up of data visualization tools (e.g. iDARTs)

• May participate in training the central study team local study team site personnel or external vendors on protocol disease evaluation criteria or other specific aspects of the clinical study

• Will actively participate in mentorship and training opportunities to expand clinical development knowledge therapeutic area expertise and leadership capabilities

Qualifications:

• Minimum of a bachelors degree in a scientific discipline is required with advance degree (i.e. MSc Ph.D. or Pharm D) preferred

• A minimum of 2 years of experience in a related clinical research position is required spending at least part of the time within the pharmaceutical industry is preferred.

• Knowledge of basic clinical research principals with an understanding of applications to drug development is required.

• Theability to work in a matrix team environment and adherence tothe highest personal and ethical standardswith a commitment to patient-centered clinical research is required.

• Fluent in written and spoken English with excellent communication skills is required.

• Working knowledge of the use of Microsoft suite of software products is required.

• Knowledge of Good Clinical Practices ICH/GCP drug development process regulatory requirements for the conduct of high-quality clinical trials including protocol development medical review oversight of study conduct data quality and safety is preferred

• Ability to travel approximately 10% domestic/international travel may be required.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via Internal employees contact AskGS to be directed to your accommodation resource.

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