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The Chief of Plants and Science will lead and integrate the horticultural and scientific initiatives at the Cleveland Botanical Garden, Holden Arboretum, and Leach Research Station, driving the quality and growth of HF&G's horticulture, living collections, research, community forestry, and conservation programs. Holden Forests & Gardens is one of the largest public gardens in the United States, offering distinct arboretum and botanical garden experiences for the public along with a private plant breeding research site.

Salary

ACTIVE

<h3>Chief of Plants and Science, Holden Forests & Gardens</h3><h3>Kittleman and Associates - Cleveland, OH, United States</h3>Posted: 01/14/25After close to a century as separate institutions, the Holden Arboretum and Cleveland Botanical Garden integrated to form Holden Forests & Gardens (HF&G) in 2014. As HF&G, the organization was restructured as a single management team in 2018, creating a dynamic and impactful plant museum spanning multiple campuses and serving the people of northeast Ohio and beyond.Holden Forests & Gardens is one of the largest public gardens in the United States, offering distinct arboretum and botanical garden experiences for the public along with a private plant breeding research site.The Chief of Plants and Science will lead and integrate the horticultural and scientific initiatives at the Cleveland Botanical Garden, Holden Arboretum, and Leach Research Station, driving the quality and growth of HF&G's horticulture, living collections, research, community forestry, and conservation programs.The Chief of Plants and Science will be a strategic and dynamic individual skilled at leading change and supporting a culture of accountability. They will represent HF&G at local and national meetings, lead tours, and serve as a spokesperson regarding plant collections, horticulture, arboriculture, science, and conservation.Minimum requirements include a master’s degree in horticulture, ecology, botany, or related plant science field from an accredited university, and 8 years’ experience in horticultural, ecological, or conservation research with at least 5 years of management experience. A Ph.D. degree is desirable. Supervisory experience in public gardens or a similar organization is preferred. A commitment to the principles of diversity, equity, and inclusion is required.The compensation range for this position annually is between $170,000 - $190,000. HF&G offers generous health insurance, retirement, PTO, and other benefits.If you would like to be a key leader in this dynamic organization, please confidentially submit a current resume and cover letter to Kittleman & Associates. The cover letter is an opportunity to showcase your passion for Holden Forests & Gardens’ vision and mission, as well as organizational impact in current or prior roles.#J-18808-Ljbffr

Gilder Search Group

Chief of Plants and Science, Holden Forests & Gardens

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JobLeads

Medical Science Liaison

The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. Consistently acts to enhance Jazz Pharmaceuticals’ image as an advocate of medical advancement by using knowledge of product, disease state and pipeline products to engage healthcare providers in meaningful scientific exchange of information.

KBSkills

If you are a current Jazz employee please apply via the Internal Career site.Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to 
transform the lives of patients and their families. We are dedicated to developing 
life-changing medicines for people with serious diseases — often with limited or no 
therapeutic options. We have a diverse portfolio of marketed medicines, including leading 
therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. 
Our patient-focused and science-driven approach powers pioneering research and development 
advancements across our robust pipeline of innovative therapeutics in oncology and 
neuroscience. Jazz is headquartered in Dublin, Ireland with research and development 
laboratories, manufacturing facilities and employees in multiple countries committed to 
serving patients worldwide. Please visit
<a href="https://www.jazzpharmaceuticals.com" rel="nofollow noopener noreferrer" target="_blank">www.jazzpharmaceuticals.com</a>
for more information.<div>The Medical Science Liaison (MSL) is a member of a field-based team of scientists who function as an extension of the US Medical Affairs organization. MSLs are responsible for developing and enhancing professional relationships with medical thought leaders involved in various phases of product development. MSLs provide medical information through scientific exchange, and clinical/scientific support for Jazz Pharmaceuticals and the Medical Affairs department.This is a field-based position covering Northern Ohio, and requires professionals with established personal and scientific credibility to interact with thought leaders and academic centers of excellence.Essential FunctionsKOL Development and Field Engagement:<ul><li>Identify and develop peer-to-peer relationships with key opinion leaders (KOLs) and healthcare providers within the therapeutic area</li><li>Develop and execute territory plans in alignment with US Medical Affairs plans</li><li>Identify and communicate key clinical and research issues and insights from KOLs to appropriate departments</li><li>Participate in medical education for healthcare professionals (HCPs) through on-site presentations at healthcare institutions, investigator meetings, national conferences, advisory boards, or regional meetings</li></ul>Provide scientific support for additional activities such as medical congress staffing, advisory boards, and sales training initiativesPositions self as Scientific Expert  <ul><li>Maintains an up to date and high-level knowledge of the therapy area, Jazz products, new and emerging areas of research, therapeutic issues and trends, and competitive landscape.</li><li>Establishes reputation as a trustworthy and knowledgeable source of scientific and medical information for the healthcare community. </li><li>Supports development of Jazz Pharmaceuticals positioning as the scientific authority in the therapeutic area. Attends appropriate scientific congresses to stay abreast of developments and to support Regional, National and local KOL activities and Jazz interests.  </li><li>Acquires a broad understanding of local and national protocols and standards of clinical practice and trends in disease management in the US.   </li><li>Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, community, and healthcare provider settings in both group and one-on-one situations</li><li>Communicates emerging data and the clinical experience with our products through scientific exchange and peer-to-peer interactions discussing benefits and risks in an objective manner.</li><li>Provide support for data generation activities (company-sponsored studies, collaboration studies, ISTs)</li><li>Provide scientific support for additional activities such as medical congress staffing, advisory boards, and sales training initiatives.</li></ul>Medical Affairs Planning and Plan Execution <ul><li>Contributes to the development of the US Medical Plan and provides input into local strategies and tactics.  </li><li>Where needed, manages relevant budget to enable execution of Medical Plan tactics as part of the wider Medical Affairs team. </li><li>Works in a collaborative manner with cross-functional colleagues to ensure a Key Account Management approach.  </li><li>Interacts with HCPs as a scientific resource to support activities aligned with the Medical Plan including advisory boards, speaker development and clinical trials. </li></ul>Responsible for maintaining Company standards and Jazz Values <ul><li>Consistently acts to enhance Jazz Pharmaceuticals’ image as an advocate of medical advancement by using knowledge of product, disease state and pipeline products to engage healthcare providers in meaningful scientific exchange of information. </li><li>Document and forward reports of adverse events and product complaints according to Jazz’s policy to ensure safe and effective use of Jazz Pharmaceuticals' products. </li><li>Adheres to the relevant national and local Codes of Practice.  </li><li>Behaves ethically and with integrity at all times.  </li><li>Acts as an ambassador for Jazz Pharmaceuticals following company mission and values.  </li><li>Keeps own written development plan and implements.  </li><li>Prepares timely reporting according to the company needs.  </li></ul>Required Knowledge, Skills, and AbilitiesRequired<ul><li>Ability to research and critically analyze and communicate complex scientific and medical information and data.</li><li>Clear and concise communication and presentation skills.</li><li>Excellent planning and organization skills, with high-level attention to detail and accuracy.</li><li>Strong strategic mindset.</li><li>Highly self-motivated and ability to work autonomously.</li><li>Ability to learn quickly, be flexible and results-focused in a rapidly changing environment.</li><li>Excellent negotiation skills.</li><li>Demonstrated skills in inter-personal relationship building, networking, collaboration and teamwork.</li><li>Strong capabilities working with digital platforms and tools are required</li><li>Excellent command of spoken English.</li><li>Ability and willingness to travel at least 60% of workdays. Driving required.</li></ul>Preferred<ul><li>Knowledge of geography, healthcare environment and external experts in academia and medical community.</li><li>Demonstrated ability to develop trust and relationships with opinion leaders in disease states of interest.</li><li>Understanding of regulatory requirements for field-based personnel</li><li>Experience in oncology</li><li>Experience as a Medical Science Liaison with a strong track record of success is strongly preferred  </li></ul>Required/Preferred Education and Licenses<ul><li>Advanced degree (PharmD, MD, PhD or equivalent) with a minimum of 3 years’ experience in the therapeutic are of interest.</li><li>License (RN, NP, CNP, PA or equivalent) with a minimum of a Master’s Degree (or equivalent) and a minimum of 5 years’ experience in clinical practice.</li><li>A minimum of 2 years’ experience as a MSL or comparable industry or clinical role is required.</li><li>This is a field position and applicants must be willing to travel 60-70% time</li><li>Valid driver’s license and live within 60 miles of a major airport</li></ul>Description of Physical Demands<ul><li>Frequent travel between meeting sites.</li><li>Frequently operating a computer, printer, telephone and other similar office machinery.</li></ul>Description of Work Environment<ul><li>Frequent interactions with external contacts in their office environment with little exposure to excessive noise, dust, fumes, vibrations and temperature changes.</li><li>Frequent computer laptop or tablet use, not usually at a workstation.</li><li>Responsibilities may require a work schedule that may include working outside of “normal” work hours, in order to meet business demands.</li><li>Frequent public contact requiring appropriate business apparel.</li></ul></div>Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.FOR US BASED CANDIDATES ONLYJazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $154,400.00 - $231,600.00Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: <a href="https://careers.jazzpharma.com/benefits.html" rel="nofollow noopener noreferrer" target="_blank">https://careers.jazzpharma.com/benefits.html</a>.

Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is an international biopharmaceutical company focused on improving patients’ lives by identifying, developing, and commercializing meaningful products that address unmet medical needs.
We have a diverse portfolio of products and product candidates, with a focus in the areas of sleep and hematology/oncology. We also support commercial products in other therapeutic areas where we can meaningfully address serious medical needs.
As part of our unwavering commitment to improve patients’ lives, we are continuing to expand our commercial product portfolio and our research and development pipeline in therapeutic areas that can leverage our unique expertise. We do this through a growth strategy of growing sales of the existing medicines in our portfolio; acquiring commercial products or product candidates that are in late-stage development; and pursuing focused development of our pipeline of differentiated therapies.

Jazz Pharmaceuticals

Medical Science Liaison, Oncology- Northern Ohio (Remote)

Adverse Events

Analysis Skills

Biotech and Pharmaceutical

Budget Management

Cancer

Clinical Data

Clinical Information

Clinical Practices/Protocols

Clinical Research

Clinical Support

Clinical Trial

Communication Skills

Community Health

Community Providers

Compensation and Benefits

Computer Workstations

Conferences

Cross-Functional

Detail Oriented

Disease

Disease Prevention and Control

Driver's License

Drug Development

English Language

Geography

Health Education

Health Information Exchange (HIE)

Health Plan

Healthcare

Healthcare Providers

Incentive Programs

Insurance

Interpersonal Skills

Jazz

Laptop PC

Manufacturing

Medical Affairs

Medical Organizations

Medical Products

Medical Records

Negotiation Skills

Neuroscience

Office Equipment

Oncology

Organizational Skills

Philosophy

Presentation/Verbal Skills

Printers

Product Development

Registered Nurse (RN)

Regulatory Requirements

Reporting Skills

Research & Development (R&D)

Research Laboratory

Research Skills

Sales

Sales Management

Sleep Disorders

Strategic Planning

Tablet PC

Team Player

Territory Development

Time Management

Trend Analysis

Willing to Travel

Appcast PX 2

MSL) is responsible for providing fair balanced, objective, scientific information, and education to opinion leaders (OLs), health care professionals, and to internal partners as required by scientific and business needs. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 <a href="#" rel="nofollow">https://www.jnj.com</a>Job Function: Medical Affairs GroupJob Sub Function: Medical Science LiaisonJob Category: People LeaderAll Job Posting Locations: Cleveland, Ohio, United StatesJob Description:Johnson & Johnson Innovative Medicine is searching for the best talent for Senior Medical Science Liaison-Neuroimmunology for the Great Lakes region. This is a field-based position located in the Great Lakes region. The ideal location is the Cleveland area, and the territory covers Ohio and Michigan.About ImmunologyOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at <a href="#" rel="nofollow">https://www.jnj.com/innovative-medicine</a>The Senior Medical Science Liaison (Sr. MSL) is responsible for providing fair balanced, objective, scientific information, and education to opinion leaders (OLs), health care professionals, and to internal partners as required by scientific and business needs. The Sr. MSL is considered an established scientific and clinical knowledge lead on current and future J&J Innovative Medicine products per Therapeutic Area (TA) alignment. The Sr. MSL is responsible for staying abreast of current scientific and treatment landscape trends in their therapeutic areas of interest. The Sr. MSL provides research support for company and investigator-initiated research. The Sr MSL will function with high integrity and follow credo values.The Sr. MSL will be responsible for:<ul><li>Building external relationships with identified KOLs and health care providers (MD, PA, NP, RN, Pharm.D., bio coordinators) and developing and managing a geographical territory. These relationships and engagements can include both virtual & in-person, with a prioritization of in-person engagements when appropriate.</li><li>Developing and maintaining a territory strategic plan, which includes educational activities with identified OLs, HCPs, institutions, and community practices.</li><li>Having a level of competency and experience in the disease state. The Sr. MSL is expected to possess foundational competencies in the areas of Influence & Results Focused, Communication, Stakeholder Engagement, Product & Therapeutic Area Knowledge, and Data Insights & Dissemination.</li><li>Rapidly identify and compliantly collaborate with field-based partners to ensure support of the Healthcare Providers which will positively impact the patients that they care for.</li><li>To enhance their skills in agility, applying the competencies of Change Management, Time Management and Innovation.</li><li>Conducting all activities in accordance with current regulatory and health care compliance guidelines.</li><li>Ability to travel, primarily throughout assigned geography, with infrequent meeting travel outside of assigned geography. Travel for this role is estimated at 60%.</li><li>Consistently demonstrating strategic territory planning and ability to build strong relationships within the territory.</li><li>Consistently demonstrating strong scientific acumen.</li><li>Continuously supporting Department Operations and Internal Partners.</li></ul>QualificationsRequired:<ul><li>A PharmD, PhD, MD, w/ 2+ years relevant neurology clinical experience.</li><li>2-3 years MSL experience, and/or 2-3 years relevant work exp (clinical or research experience) and/or related pharma work.</li></ul>Preferred:<ul><li>Knowledge or experience in Neurology, Immunology or Neuromuscular.</li><li>Launch experience in rare disease.</li><li>Significant experience giving presentations.</li></ul>Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.#LI-Remote#J-18808-Ljbffr

Caring for the world, one person at a time... inspires and unites the people of Johnson&nbsp;&amp;&nbsp;Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson&nbsp;&amp;&nbsp;Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

Our Family of Companies comprises:

 The world’s sixth-largest consumer health company. 
 The world’s most comprehensive medical devices business. 
 The world’s sixth-largest biologics company. 
 And the world’s fifth-largest pharmaceuticals company. 


We have more than 265 operating companies in more than 60 countries employing approximately 126,500 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

Johnson & Johnson

Senior Medical Science Liaison-Neuroimmunology-Great Lakes

The Product Steward Labeling Specialist is responsible for supporting the Marketing Product Information group along with MCC Labeling for all pertinent and compliant labeling information needed on a label for North America. This may also include working with the technical team to run experimental product comparisons to current formulation of product to determine if a label needs updating for compliance.

About UsPace® Life SciencesPace® makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP commercial product support. For customers with in-house manufacturing and labs, Pace® provides professional services to support their operations. Job DescriptionMake an impact. Build a career.At Pace®, everything we do is built upon an unwavering commitment to making the world a safer, healthier place. We continually work to develop innovative practices that drive sustainability and empower our partners with accurate, quality data at every critical moment and milestone. That’s why we need you — your curiosity, your talents, and your drive — to help us advance this important work, and your career. Find your place at Pace®Join us as a Product Stewardship labeling Specialist, where you’ll put your love of science to work in the Scientific Insourcing department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The Product Steward Labeling Specialist is responsible for supporting the Marketing Product Information group along with MCC Labeling for all pertinent and compliant labeling information needed on a label for North America. They will work with the current team to review and approve labels for the MOC projects, along with labels being updated for GHS Rev 7 addition in Canada for 2025 and for the US in 2026. This may also include working with the technical team to run experimental product comparisons to current formulation of product to determine if a label needs updating for compliance. This position will work with fellow team members to evaluate, review, and update labels for all incoming regulation updates. This position will also be responsible for completing CCCR reviews and creating label templates for our label printing team. This position may work with the Procurement Department to review AP products to client standards and current regulations to determine if products can be sold from the client locations. We are looking for someone who can be part of a team, but also work independently when necessary. This position will need to manage multiple tasks along with working in multiple software  NOTE: This is a hybrid position after the first 30 days of training onsite.  Then 3 days working onsite and 2 days working remotely. What you’ll do LABEL REVIEWS<ul><li>Complete CCCR reviews and label templates to be used by the label printing team</li><li>Complete label reviews for FHSA and OSHA labels</li><li>Work with technical for label review comparisons and timelines for label updates</li><li>Identify areas of improvement for efficiency</li><li>Work with Product Information for approval of labels</li></ul>PROCUREMENT / AP APPROVALS<ul><li>May work on requests for products to be sold in stores from Procurement</li><li>Research product and review SDS, VOC, and where product will be sold</li><li>Verify the product is compliant for region being sold</li></ul>PROCESS DOCUMENTATION<ul><li>Document and track all label reviews</li><li>Document and track all CCCR requests</li><li>Document and track all experimental comparison requests</li><li>Document and track all Procurement requests</li><li>Work with team members on all final approvals</li></ul>What you’ll bring<ul><li>Bachelor's degree in Chemistry, Biochemistry, Biology or related science.</li><li>Proficient in MS Office products, especially Excel</li><li>Ability to learn new software programs quickly</li><li>Good multitasking and time management skills</li><li>1-2 years of Chemical regulatory experience, Preferred</li><li>Familiarity and understanding of Regulations governing chemicals, their use, environmental impact, and associated hazards in the coatings industry (ex. VOCs, GHS, etc), Preferred</li><li>Laboratory/Formulation Experience, Preferred</li><li>Experience with existing customer compliance software (ex: HEARS), Preferred</li><li>Knowledge in managing regulatory and stewardship requirements for business(es), Preferred</li></ul>#LI-RG1 Additional Information<div>Benefits80 hrs of paid vacation per year, 7 paid holidays per year, 2 floating holidays per year (prorated based on start date), 40 hrs paid sick time per year, paid bereavement leave (days based on relation to the employee), 8 hrs paid volunteer time per year, parental leave, medical, dental, vision, voluntary short-term disability, long-term disability, life insurance, voluntary supplemental life insurance, traditional 401k and ROTH 401k with a company match, HSA, FSA, employee referral bonus, employee assistance program, tuition reimbursement program, employee recognition program, voluntary ID theft coverage, voluntary legal coverage, voluntary accident insurance, voluntary hospital indemnity insurance, and voluntary critical illness insurance. Equal Opportunity EmployerPace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.</div> Work Schedule Monday through Friday 8-5pm (Flexible)

Pace® Life Sciences

Product Stewardship Labeling (Hybrid)

Accounts Payable

Biochemistry

Biology

Chemistry

Customer Support/Service

Environmental Impact

GMP (Good Manufacturing Practices)

Industrial Coating

Insourcing

Laboratory

Marketing

Microsoft Office

Multitasking

OSHA

Operational Support

Printing

Product Reviews

Product Support

Professional Services

Purchasing/Procurement

Regulations

Stewardship

Sustainability

Work From Home

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