Pharmaceutical Clinical Associates, LLC
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Raritan,
NJ
As Chief Medical Officer, you will be part of the Senior Management Team-- setting strategic goals for the Company; broadening existing relationships (yours and ours) within the industry and among oncology clinical researchers; bridging business opportunities with operational planning and execution.
As CMO, you will be the primary scientific and medical voice of the Company drawing clients to our organization by your knowledge, experience, partnership, and idea-sharing. You will be expected to represent Company on the industry stage as a leader in successful clinical trial conduct. You will seek to build relationships with potential clients; industry organizations; and investigators. You will develop presentations for and present at oncology-focused meetings, at client presentations; in workshops; and for the advancement of internal training. You will be encouraged to write and publish articles in trade journals and, as possible, in scientific journals. Working with Business Development team members, you will use your industry, medical and oncology background to attract and develop oncology opportunities.
Your insight into clinical trial conduct, your desire to make an impact on the conduct of clinical trials in oncology, and your entrepreneurial, innovative spirit will drive Company to breakthroughs in the conduct of clinical trials in oncology and other complex therapeutic Company areas. You will partner with site investigators to find creative solutions to roadblocks in trials. As expands further globally, you will work with global partners to develop delivery strategies and study solutions for completion of projects that meet goals of timing, budget, and data integrity. You will act as a Scientific Liaison to staff as well as to clients; provide medical consultation as required/requested to client/sponsor or other service groups; conduct study protocol feasibility reviews; assist in the evaluation of clinical development plans with sponsors and may function in the capacity as a Safety Officer and Medical Representative on the project teams if needed.
A. Serve as an oncology expert and business development resource to increase the Company’s position in the oncology marketplace.
Ø Provide consultative input to clients/potential clients regarding product development plans, study protocols and other projects.
Ø Collaborate with thought-leaders and professional faculty to best design and implement projects.
Ø Monitor safety data and efficacy trends by reviewing clinical data.
Ø Design clinical portions of INDs, NDAs, BLAs (including protocols, IBs, medical reports, Safety and Efficacy summaries, scientific rationales, and benefit-risk ratios)
Ø Visit Company clients or potential clients 4 – 5 days per month
Ø Network with database of Industry contacts and expand database of Clinical contacts.
Ø Participate in Strategy Meetings once a quarter.
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Attend and present materials, as needed, at meetings with Company as well as extra-company meetings (ex: Investigator Meetings).
Ø Publish articles
Ø Participate in brainstorming sessions to develop solutions for projects.
C. Effective, accurate, and concise communication expertise with multiple levels of the organization.
Ø Close attention to detail with absolute commitment to quality: ability to maintain a
high-quality/ outstanding department reputation in order to acquire new and
repeat business.
Ø Appropriately represent Beardsworth when building and maintaining relationships with clients, sites, and vendors; ability to build trust and confidence in teams/departments.
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Pharmaceutical Clinical Associates is always accepting employment inquiries from professionals interested in our opportunites. If you are interested in career opportunities at Pharmaceutical Clinical Associates please use our online resume formto apply. Pharmaceutical Clinical Associates is an Equal Opportunity Employer.
Raritan, NJ
Raritan, New Jersey
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