Jobs for People with MS: National MS Society

Associate Director, Clinical Physician - 2407021182W

Description

Kenvue is currently recruiting for:

Associate Director, Clinical Physician

This position reports into the Senior Director, Clinical Operations and is based in Paranaque City.

Who We Are

At Kenvue (https://kenvue-my.sharepoint.com/personal/KAbaca_kenvue_com/Documents/JDs/Marketing/Final_from Penn/kenvue.com/careers) , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information click here. (https://www.youtube.com/watch?v=XhsbOsBiX_M)

What You Will Do

The Associate Director, Clinical Physician will be responsible in ensuring that human research studies are conducted in compliance with regulatory requirements and that participant safety is always the top priority. He/She will lead a team to provide oversight and medical monitoring for human research studies.

Key Responsibilities

• Lead a team of physicians who act as the primary medical monitor for human research studies globally, including market research and clinical studies

• Leader of global process and procedures to ensure adequate and compliant medical monitoring of human research studies, working closely with cross-functional teams

• Develop and implement risk management strategies to ensure participant safety

• Conduct documented review and interpretation of adverse event/safety data and identify and escalate potential safety issues per appropriate procedures

• Maintain accurate and complete records of all safety-related activities

• Determine eligibility of reports in instances where the Principal Investigator is not medically qualified.

• Participate in safety review meetings and provide expert medical advice to clinical teams

• Prepare and review safety reports and other documentation required for regulatory submissions

• Collaborate with cross-functional teams, including clinical operations, clinical scientists, biostatistics, data management, medical safety and regulatory affairs

• Stay current with the latest safety regulations and guidelines globally and ensure that human research studies are conducted in accordance with these standards

• Provide training and guidance to other team members as needed

Qualifications

What We Are Looking For

Key Qualifications

• A medical degree (MD or equivalent) is required.

• At least 7 years of experience in clinical development and safety monitoring, including experience in leading teams, within the consumer health or pharmaceutical industry

• Knowledge of global clinical trial regulations, safety regulations and guidelines, including ICH guidelines

• Experience with safety monitoring in clinical studies, including pharmacovigilance and risk management

• Experience in being part of a global team, including leading teams

• Highly passionate in making a positive impact in our consumers’ lives

• Proficient in Microsoft applications including Outlook, Word, Excel, Project, and PowerPoint

• Awareness and willingness to work within Medidata Rave and Veeva platforms

• Must have excellent communication skills in English (both oral and written) and be able to work independently and effectively as part of a cross-functional teams both internally and externally to the organization

• Ability to manage multiple projects simultaneously and prioritize tasks

• Attention to detail and ability to work with large amounts of data

• Willingness to adapt to changing priorities and assignments

• Demonstrated ability to develop and work within agile processes and business frameworks

What’s In It For You

• Competitive Benefit Package

• Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!

• Learning & Development Opportunities

• Employee Resource Groups

• Flexible Work Arrangements

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location Asia Pacific-Philippines-National Capital-Paranaque

Job Function Clinical Research non-MD

Req ID: 2407021182W