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Post by sluggobear on Apr 26, 2016 0:02:17 GMT -5
And Peppy - the optimistic side of me wants to believe!!: that the good guys DO win in the end, that we should always fight the good fight, and that the cheaters and thieves and frauds of life eventually fail and go to jail (Hamburg, Shkreli, Fraudstain). Yes I AM tired of little pricks! Good luck to the good guys.
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Post by lakon on Apr 26, 2016 14:01:52 GMT -5
In 1961 President John F. Kennedy addressed the Canadian Parliament. The President said, "At the conference table and in the minds of men, the free world’s cause is strengthened because it is just. But it is strengthened even more by the dedicated efforts of free men and free nations. As the great parliamentarian Edmund Burke said, 'The only thing necessary for the triumph of evil is for good men to do nothing.'”
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Post by Deleted on Apr 30, 2016 9:15:29 GMT -5
More new positions listed in the corp careers
Regional Sales Manager, Mid-West Area Regional Sales Manager, South-West Area Regional Sales Manager, North-West Area
Regional Sales Manager, Mid-South Area
Regional Sales Manager, North-East Area Regional Sales Manager, South-East Area
MannKind Corporation is currently seeking for a Regional Sales Manager Mid-West Area. In this position the incumbent will be responsible for development and management of a region with the goal of maximizing sales. Lead, direct and manage the activities of sales representatives with a geographic area. Lead the team to achieving established revenue and profit goals. Manage expenses in a fiscally responsible manner. Participate in national, regional, and local strategic meetings as well as lead meetings with respective team.
Proven ability to motivate and coach sales team to meet goals and objectives through influencing behavior Lead a team of Sales Representatives to promote product(s) to targeted physicians and account to achieve/exceed specific business goals Work with Sales Representatives on a consistent basis, evaluating, coaching and directing sales presentations Attract, coach and retain individuals who will ensure high level performance Direct the Area Sales Manager in the acquisition, expansion and retention of targeted business within the assigned geographic area Develop plans that effectively translate national strategy at the District level Work with Leadership to define and establish appropriate behaviors and actions that will lead to sales growth acceleration in the geographic area Fully engage with key customers by developing and implementing strategies that support the growth of assigned product(s) Participate in and contribute to commercial team planning sessions as requested, representing the needs of customers and the sales team and driving business building plans of the organization Operate within Compliance Guidelines at all times Responsible for observing all Company, Health, Safety and Environmental guidelines
Duties and responsibilities are not limited to the work listed above and may include other assignments as necessary.
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Post by bradleysbest on May 2, 2016 16:07:14 GMT -5
As far as sales reps go, am I correct in assuming they will receive incentive based bonuses including MNKD stock options?
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Post by mnkdnewbie on May 5, 2016 17:15:21 GMT -5
2 new jobs posted:
Global Safety Officer
VP North American Medical Affairs
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Post by 4877377al on May 5, 2016 17:46:32 GMT -5
Looks to me like Matt is creating a number of "big cigar" jobs, but lets hope he has the matches for the cigars! Whomever has been running down share price and employing all of the hatch man to post, truly is out to destroy MNKD. Its become a vendetta of desperation by BP!
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Post by Deleted on May 5, 2016 18:05:19 GMT -5
rew12.ultipro.com/MAN1011/JobBoard/JobDetails.aspx?__ID=*02B6F58C71F91651VP - North America Medical AffairsDescription MannKind Corporation is currently seeking a Vice President of North America Medical Affairs. The VP of N.A. Medical Affairs will be responsible for overseeing the medical affairs function reporting to the Chief Medical Officer. Work with various internal functional areas, including marketing and sales, to identify and capitalize on current and future business opportunities based on changes in the medical and regulatory environment. Oversee the clinical and regulatory departments in the planning, execution and management of clinical trial activities, compliance, legal and regulatory activities to ensure standard operating procedures are followed. Recommend strategies and implement functional plans in accordance with the company’s long term strategic and financial goals, inkling but not limited to information and data relating to hospital, medical, health and governmental planning issues. Maintain positive professional relationships with the medical community, especially in MannKind’s specific discipline/product line to identify future business opportunities and emergency medical and health care practices. As MKC’s primary information, industry and governmental liaison, keeps the organization informed on emerging trends, issues and business forecasts. May facilitate and/or deliver scientific/medical exchanges of information, or clinical and research findings of products through symposia, lectures and publications.
Develop innovative, consistent, and clear strategies for the company by integrating all medical and scientific data pertaining to efficacy, safety and dosage, from discovery to post-marketing Produce position papers on scientific and medical content regarding Company products, competitors’ products and clinical trials, regulatory guidelines, etc Shape medical and scientific opinion of key stakeholders (i.e. FDA/EMA, KOLs, and guideline-making bodies). Continue to build the Company’s core competency in product design. Work in close coordination with Clinical, R&D, Commercial, and Regulatory Ensuring the world-class stature, relevance, completeness, quality, and effectiveness of medical and scientific messages, information, and data used in communicating with Company customers, users, and regulatory authorities Provide therapeutic area expertise and medical input into the formulation of the overall development and global commercialization strategy Establish strong relationships with KOLs. Work with healthcare systems and payors to drive changes in the hospital treatment care pathways Provide medical leadership into the development of a communication and publication strategy, including overseeing the medical content of all materials such as publications, manuscripts, abstracts, posters, education, marketing, etc. Ensure that the content of medical Symposia Congress presentations are accurate, strategically focused, and compliant Provide medical review for the medial information, educational slides and letters for healthcare professionals, and the review of marketing materials Develop and implement a strategic staffing plan for Medical Affairs activities and the MSL team as needed Develop and implement Medical Affairs training programs in preparation for product(s) launches and ongoing educational needs Represent the company at medical meetings, advisory boards, outreach meetings at key institutes, and in interactions with KOL’s Monitor and oversee safety, including the ongoing safety signal detection for the clinical programs Responsible for observing all Company, Health, Safety and Environmental guidelines
Duties and responsibilities are not limited to the work listed above and may include other assignments as necessary.
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Post by Deleted on May 5, 2016 18:07:27 GMT -5
rew12.ultipro.com/MAN1011/JobBoard/JobDetails.aspx?__ID=*CC07B12A90BEFAC9Global Safety Officer MannKind Corporation is currently seeking a Global Safety Officer. The Global Safety Officer will be responsible for managing and overseeing MannKind’s drug safety and pharmacovigilance process. Manage compliance with standard operating procedures, regulatory safety and pharmacovigilance in compliance with national and international regulations, such as the Food and Drug Administration (FDA) and World Health Organization, global, regional and country regulations for the reporting of adverse events to regulatory agencies. Coordinate the development of guidelines and ensures the uniform and timely processing of adverse event reports. Interfaces with internal and external collaborators to develop programs and processes to meet regulatory reporting requirements. Oversee the development and preparation of reports for company management as well as external regulatory agencies. Manage and conduct ongoing safety surveillance on company products. Oversee the preparation of new drug application safety updates, investigational new drug safety reports, investigator communications, and product labeling/package inserts and other reports as necessary. Participates in oversight of ongoing clinical trials and in the preparation of new drug applications with respect to drug safety.
As the Senior PV leader, provide a strong, clear voice for the PV function including development of a global PV management system Provide strategic consultation and guidance on all decisions that have significant drug safety implications Establish, maintain, direct and communicate a global benefit-risk strategy for each pre-market, marketed and future MannKind product that includes risk management and minimization Establish metrics to monitor the PV system and ensure maintenance of internal and external regulatory compliance to the highest standards Oversee the implementation and maintenance of a global drug safety database capable of expedited and periodic reporting of safety data in accordance with current global regulatory requirements Oversee the implementation and maintenance of a global safety signal detection system that includes tracking of signal evaluation, outcome and communication Provide PV contributions in efforts to secure global regulatory approvals Be accountable for the acquisition, processing, storage, retrieval and distribution of information concerning SAEs in clinical trials Collaborate closely with Research, Preclinical, Clinical, Regulatory Affairs and Medical Affairs to ensure tight strategic integration of drug safety plans Closely supervise all major written deliverables (regulatory submissions, original articles, abstracts), and presentation materials that contain drug safety information Prepare safety information to support licensing partners and contract research organizations, review safety documents prepared by licensing partners and contract organization, and communicate with licensing partners and contract organizations on safety matters per agreements Ability to work cross-functionally to liaise between the PV team and other departments, external service providers and contract manufacturers Accountability for adherence to relevant regulatory requirements and company SOPs as appropriate Responsible for observing all Company, Health, Safety and Environmental guidelines
Duties and responsibilities are not limited to the work listed above and may include other assignments as necessary.
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Post by Deleted on May 5, 2016 18:08:14 GMT -5
^^ Looks like the CMO got some budget $$$ to expand his department
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Post by mnkdnewbie on May 5, 2016 18:19:22 GMT -5
^^ Looks like the CMO got some budget $$$ to expand his department Maybe rls used technosphere to grow money trees, really big ones like on the their homepage.
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Post by Deleted on May 5, 2016 19:01:42 GMT -5
^^ Looks like the CMO got some budget $$$ to expand his department Maybe rls used technosphere to grow money trees, really big ones like on the their homepage. any $$$$ from RLS is material and will be filed by Mannkind
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Post by bradleysbest on May 5, 2016 23:32:11 GMT -5
Anyone know if any of these new jobs have been filled yet?
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Post by lakers on May 6, 2016 17:03:37 GMT -5
SNY settlement may come first. Matt will explain the funding source for those new hires and open reqs.
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Post by mnkdnewbie on May 6, 2016 18:15:26 GMT -5
SNY settlement may come first. Matt will explain the funding source for those new hires and open reqs. Where have you been lakers?
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Post by patten1962 on May 6, 2016 20:18:28 GMT -5
SNY settlement may come first. Matt will explain the funding source for those new hires and open reqs. will this happen Monday?
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