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Associate Director, Clinical Project Scientist (1 of 3) - 2306112251W

Description

Janssen Research & Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for an Associate Director, Clinical Project Scientist located in Raritan, NJ. Remote locations within the United States may be considered on a case-by-case basis and if approved by the company.

At the Janssen Pharmaceutical Companies of 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.

Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, cardiovascular and metabolism, and pulmonary hypertension. Please visit http://www.janssenrnd.com for more information.

The Associate Director, Clinical Project Scientist will be a responsible member of a clinical team dedicated to the development and execution of clinical strategies and the clinical and operational implementation of a complex compound program. This individual will provide active scientific contribution to a cross-functional clinical team developing a molecular entity. Provide input to the clinical development plan, work on the development of the clinical trial protocol, clinical trial materials, and take responsibility for coordinating completion of clinical study reports and support preparation of relevant documents for regulatory filings. This role will involve extensive team matrix interactions with colleagues from a number of different disciplines. This individual may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area.

Principal Responsibilities:

• Support preparation of clinical development plans, trial protocols, and support the operations group with trial set up and monitoring and assist with completion of clinical study reports.

• Assist Physicians in the evaluation of adverse events (pre and post-marketing) for relationship to treatment and support the interpretation and reporting of results.

• Assist Regulatory Affairs in determining requirements for any corrective actions or Health Authority (HA) reporting.

• Interpret, report and prepare oral and written results of product research, in concert with senior clinical personnel, in preparation for HA submissions.

• Perform data review in conjunction with other clinical team members.

• Assist Regulatory Affairs in the development of drug regulatory strategies.

• Participate on and may lead cross-functional teams for evaluation of new product ideas, implementing franchise business strategies, etc.

• Review medical literature and related new technologies.

• May be asked to lead the execution of contracts.

• May be asked to assess medical publications emerging from the team and its affiliates.

• May be responsible, with appropriate colleagues, for the review of company advertising and promotion.

Qualifications

• A minimum of a Bachelor's degree is required, preferably in Biological Sciences or Nursing. An advanced degree (e.g., Master’s, PhD or PharmD) is preferred.

• A minimum of 6 years of clinical research and development experience within the pharmaceutical industry is required.

• Extensive experience with managing/supervising clinical trials and clinical research programs is required.

• Experience in the cardiovascular and metabolism Therapeutic Area preferred.

• Experience building cross company alliances preferred.

• Must have strong interpersonal and communication skills.

• Must have the ability to work well in a dynamic team environment and be able to prioritize and respond to changing needs of the business.

• The ability to collaborate with all levels and influence decision-making across a matrix organization is required.

• This position will require up to 10% travel is required.

The anticipated base pay range for this position in the San Francisco Bay Area, CA is $150,300 to $259.210.

The anticipated base pay range for this position in all other US locations is $131,000 to $225,400.

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.

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)).

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

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

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

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.

Primary Location NA-US-New Jersey-Raritan

Other Locations NA-United States

Organization Janssen Research & Development, LLC (6084)

Relocation Eligible: No

Job Function Clinical Research non-MD

Req ID: 2306112251W