Senior Director, Clinical Pharmacology - Doral, United States - QPS Holdings, LLC

Description

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you We are currently seeking a talented Senior Clinical Pharmacologist with late phase experience to join our dynamic team and contribute to design, oversight and interpretation of clinical studies that drive forward our clients drug development strategies.

QPS' Story:

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services.

To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.

Team members enjoy challenging and rewarding work, and are encouraged achieve their best.

Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded.

We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today
Please visit our website ) for more information and to see all current openings.
The Job

• Supervises clinical studies from a clinical pharmacology and scientific perspective.
• Develops and maintains a global network of experts to support clinical studies.
• Initiates and coordinates strategic initiatives to maintain and improve Clinical strength at QPS.
• Initiates, coordinates, or writes scientific publications.
• Reviews and discusses the feasibility of client requests for late phase clinical studies based on scientific design and Client needs.
• Provides input on designs of clinical studies for any of QPS facilities considering both scientific and operational aspects.
• On request develops study designs for clinical pharmacology studies. The Senior Director Clinical Pharmacology will work in close collaboration with subject matter experts (internal or external) and local QPS sites.
• Supports Business Development in the acquisition process and participation in sponsor visits and attendance of scientific meetings or bid defense meetings to represent QPS.
• Consults with Sponsor on clinical studies and clinical development programs.
• Will on request be involved in evaluating the feedback of the sponsor and QPS performance and advise in taking the desired actions to be in line with scientific and Sponsor needs.
• Maintains contact with other QPS site managers/staff on aspects of clinical development projects/studies relevant for that site.
• Be involved in the CSR writing and reviewing process e.g. by writing discussion sections of the CSR if applicable, review of the CSR and discussions with the sponsor on review comments.
• Advice Clinical executive management on strategic developments in the Clinical Pharmacology field.
• Keeps an up-to-date knowledge on relevant international and local law and guidelines for conduct of clinical pharmacology studies at any of QPS' facilities.
• Advise on study feasibility based on pharmacology, preclinical safety, pharmacokinetics and pharmaceutical aspects of the compound and QPS' expertise and capacities.
• Advise project teams on the execution of the clinical studies to guarantee flawless conduct of study. After completion of studies, support in evaluating study and performance as lessons learned activities.
• If necessary, advise on processes, staffing and systems to improve study quality and customer satisfaction.
• In addition to these tasks, other tasks (undisclosed) can be executed as well to the Senior Director Clinical Pharmacology upon discussion with Global Medical Affairs.

Work Location

• This job may be 100% home-office based. (see Telecommuting Policy for full details)
• Travel responsibilities are expected.

Requirements

• PhD degree in medical, pharmaceutical, or biological sciences.
• 15 years relevant work experience in clinical pharmacology and project management in a function as Clinical Pharmacologist, Scientist, Research Physician or a comparable function in clinical research.

Why You Should Apply

• Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
• Structured Career Ladders that provide excellent growth based on your personal aspirations.
• Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
• Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance
• Park-like setting in Newark, Delaware
• Internal committees designed with the needs and enjoyment of QPS employees in mind.

QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer.

In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law.

Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

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