Senior Clinical Trial Specialist

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

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

R&D Operations

Job Sub Function:

Clinical Trial Support

Job Category:

Professional

All Job Posting Locations:

Cincinnati Ohio United States of America Santa Clara California United States of America

Job Description:

Clinical Affairs of Robotics and Digital Solutions Johnson & Johnson MedTech is recruiting a Senior Clinical Trial Specialist. This role is responsible for leading operational activities of clinical trials well as encouraging strong positive relationships with colleagues across the organization.

The Senior Clinical Trial Specialist ensures inspection readiness through compliance with the clinical trial protocol company Standard Operating Procedures (SOPs) Good Clinical Practices (GCPs) and applicable regulations and guidelines from study start-up through clinical study report. The Senior Clinical Trial Specialist will conduct site monitoring activities for clinical trials as well as operational aspects of studies.

At Johnson & Johnson we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented treated and cured where treatments are smarter and less invasive and solutions are personal. Through 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 humanity. Learn more at MedTech

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at Job Activities:

• Executes and leads clinical trials ensuring compliance with timelines and study milestones.
• Oversees/drives feasibility selection set up conduct and closure of a clinical trial within the allocated countries in accordance with the ICH-GCP applicable legislation and Company SOPs
• May serve as the primary contact for trial sites (i.e. site management).
• Develops clinical trial documents (e.g. study protocol informed consents CRF monitoring plan study manual investigator brochure annual reports).
• Ensures applicable trial registration (e.g. on) from study initiation through posting of results and supports publications as needed.
• Manages/coordinates ordering tracking and accountability of investigational devices and trial materials.
• Partners and collaborates with site personnel IRBs/ECs contractors/vendors and company personnel.
• Interfaces with collaborates with and is responsible for Clinical Research Associates (CRAs).
• Coordinates and supports the development and execution of Investigator agreements and trial payments.
• Is responsible for clinical data review to prepare data for statistical analyses and publications.
• May perform monitoring activities including site qualification visits site initiation visits interim monitoring visits or close out visits based on study need.
• Ensure site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.
• Ensure that all Adverse Events (AE) /Serious Adverse Events (SAEs )/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropriate. For AEs/SAEs ensures that they are consistent with all data collected and with the information in the source documents.
• May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS) with collaborative relationships with all relevant Clinical partners and cross-functional partners (e.g. Global Strategic Marketing Medical Affairs Regulatory Affairs Health Economics and Market Access R&D etc.) contributing to cross-functional alignment.
• May provide on-site procedural protocol compliance and data collection support to clinical trial sites.
• Independently solves problems arising during clinical study execution and will seek guidance for more complex problems as needed.
• Responsible for communicating business related issues or opportunities to next management level.
• Knows understands incorporates and follows all applicable laws and regulations relating to J&J business activities and Policies and Procedures of the Health Care Compliance Program and Code of Conduct.
• May be asked to provide additional support for the trial team as needed.

Qualifications:

Education

• A minimum of a Bachelors degree and/or equivalent University degree is required; focused degree in Life Science Physical Science Nursing or Biological Science discipline is preferred.

Experience

Required:

• A minimum of 4 years of professional work experience (6 years preferred)
• Previous clinical research experience required.
• Previous medical device site monitoring or equivalent experience required.
• Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products.
• Experience and knowledge working with computer systems (Microsoft Office Excel Word Power Point and Outlook).
• Strong digital literacy in appropriate software and related company clinical systems.
• Good understanding of clinical research science and processes along with an understanding of clinical trends and global clinical trial regulations.
• Proficient in speaking and writing the country language English.
• Presentation and influencing skills.
• Strong organizational skills (e.g. able to handle multiple sub-projects and tasks simultaneously and consistently meet all associated metrics).

Preferred:

• Medical background preferred.
• Relevant industry certifications preferred (i.e. CCRA RAC CDE).

Other:

• May require up to 30% domestic and/or international travel to other sites and locations

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

Required Skills:

Preferred Skills:

Clinical Data Management Clinical Evaluations Clinical Research and Regulations Clinical Trial Protocols Clinical Trials Operations Communication Data Savvy Empowering People Issue Escalation Laboratory Operations Problem Solving Program Management Project Support Research and Development Standard Operating Procedure (SOP) Study Management Technical Credibility

The anticipated base pay range for this position is :

$109000.00 - $174800.00

For Bay Area:

$125000.00 - $201250.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).

For additional general information on Company benefits please go to: - position is eligible to participate in the Companys long-term incentive program.



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