Johnson and Johnson is recruiting for a Manager, Clinical Science; Immunology Therapeutic Area, to be located in Spring House, PA. Remote work options may be considered on a case-by-case basis and if approved by the Company.
At Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found.
Johnson & Johnson discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit http://www.JanssenRnD.com for more information.
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Johnson and Johnson Immunology has a history of bringing life-changing therapies to patients with immune-mediated diseases.
The focus of the Manager, Clinical Scientist is to support various clinical research tasks associated with assigned Immunology Development clinical trials, program execution, innovation, and optimization of execution. Scope of work will include tasks associated with the execution, monitoring, and reporting results of clinical trials evaluating therapeutics in immunologic disorders. The range of tasks may vary to some degree depending on the therapeutic area and trial-specific requirements.
The Clinical Scientist is a key member of development clinical trial teams, works in collaboration with Study Responsible Clinical Scientist and in partnership with Project Physician(s). The Clinical Scientist provides active scientific contribution to a cross-functional clinical team developing a molecular entity. Provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, supports completion of clinical study reports and preparation of relevant documents for regulatory filings. This role involves extensive team matrix interactions with colleagues from different disciplines.
Responsibilities include:
- Supports activities related to the design, execution, monitoring, and reporting of clinical trials.
- Supports preparation of clinical development plans, trial protocols, case report forms, study operational plans
- Supports medical monitoring activities and reporting in partnership with Study Responsible Clinical Scientist and Study Responsible Physician, evaluates clinical trial adverse events, reviews clinical laboratory results, drafts adverse event narratives.
- Partners with Clinical Operations in trial set up, conduct, recruitment activities, closeout, and reporting
- Assists Data Management with the review of clinical data and query resolution
- Works closely with Quality Management & Assurance to ensure flawless execution of clinical trials
- Supports completion of clinical study reports
- Supports responses to questions from Ethics Committees and Health Authorities
- Supports integrated document development for marketing authorization filing and preparation for the FDA Advisory Committee and EU Oral Explanation
- Reviews medical literature and related new technologies
Qualifications
- BS, MS, PharmD, PhD or RN preferably with a scientific background in Immunology or a related field, and 5 years industry experience or equivalent clinical research experience is required.
- Experience in late-stage drug development, experience in immuno-inflammatory indications is preferred.
- Ability to survey and interpret the scientific literature related to the assigned projects is required.
- Strong organizational skills and the ability to work well in a dynamic environment and be able to prioritize and respond to changing needs of the business.
- Good interpersonal skills and the ability to advise, persuade, and negotiate with colleagues in a supportive and encouraging fashion.
- Excellent written and verbal English communication skills.
- The ability to work in a global matrix organization with cross-functional teams is required.
- Proficient with Microsoft Office applications EXCEL, POWERPOINT, and WORD.
- 10-20% domestic/international travel may be required.
The anticipated base pay range for this position is 115000 to 197800. California Bay Area - The anticipated base pay range for this position is 141000 to 227700.
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis. • Please use the following language:
- Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
- Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
- This position is eligible to participate in the Company's long-term incentive program.
- Employees are eligible for the following time off benefits:
- Vacation - up to 120 hours per calendar year
- Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year
- Holiday pay, including Floating Holidays - up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar year
- Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits
The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.
Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.
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