Sr. Clinical Research Specialist

Mentor Corporation, a member of the Johnson & Johnson Family of Companies, is currently recruiting a Sr.

Clinical Research Specialist located in Irvine, CA.



*There is already an identified candidate for the role.

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 https://www.jnj.com/ .

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.

Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.

Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.

Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

Job Description:

Serves as an expert on clinical trial matters and provides governance on clinical trial operations.

Defines parameters for the clinical support team and leads the data collection process on patients and prospective participants.

Compiles statistical and metric data based on clinical activities.



* Utilizes clinical trial best practices to ensure the safety and confidentiality of all study subjects in clinical activities.



* Applies in-depth knowledge and experience to carry out corrective and preventative actions designed to mitigate risks in trials.



* Categorizes data from clinical trials according to stakeholder specifications and generates reports for leadership.



* Documents clinical trial findings and examines data accuracy through computer data analysis programs and on-site and remote monitoring.



* Communicates internally and externally as a site-processes specialist to inform stakeholders, clients, and other relevant parties of clinical trial activities.



* Observes and trains patients on trial purpose and outcomes in accordance within all regulatory requirements.



* Coaches more junior colleagues in techniques, processes, and responsibilities.



* Understands and applies Johnson & Johnson's Credo and Leadership Imperatives in day-to-day interactions with team.

The anticipated base pay range for this position is $104,000 to $166,750.

The Company maintains highly competitive, performa...