We have an exciting opportunity for a Medical Liaison-Oncology to join a small company within a global pharmaceutical company that is driven by scientific innovation that touches patients' lives worldwide.
Organizational Attributes:
- Join a global company with a culture that values collaboration, diversity, scientific ingenuity, curiosity, discovery, and breakthrough innovation.
- They provide fantastic opportunities to grow, develop new skills and, and share your best ideas in a fast-moving and engaging environment.
- They are among Fortune Magazine’s most admired companies.
- They are voted as an employee of choice by publications outside the industry.
- Builds long-term professional relationships and advocacy; and secures contributions from Decision-makers, Medical Experts, and Health Care Professionals.
- Identifies potential research opportunities that align with medical and business strategies including preclinical and translational research and epidemiology projects.
- Educates Health Care Professionals, Regulatory Agencies, and Federal stakeholders on trending data and pipeline platforms.
- Offers medical support as a part of a cross-functional team to clinical trials.
- PharmD, PhD, or MD or a doctoral degree required.
- 2 years oncology postdoctoral liaison experience.
- Knowledge of oncology clinical medicine, medical research, disease management in at least one therapeutic discipline.
- Knowledge of oncology clinical medicine, disease management and medical research in at least one therapeutic area.
Job Features
| Job Category | Pharmaceutical |
| Reference Number | 3-5-20SW |
| Salary | Competitive |
Located in one of the most desirable communities in Florida is an iconic global leading pharmaceutical company that develops and distributes orthopedic solutions across the globe.
We are searching for a Clinical Research Associate with solid experience in the medical device field; orthopedic experience will be an advantage.
The company provides relocation assistance and offers remote working opportunities for qualified candidates.
Why join this organization:
This Leading Medical Device Company is privately owned, boasts impressive double digit year over year growth, and has a vision to establish itself in the public space and grow to become a $1Billion Company!
Outstanding location!
- Live and work in a community in Florida consistently rated as one of the nation’s most livable cities offering
- Reasonably priced and high-quality housing
- No state income tax
- Outstanding schools, and nationally recognized healthcare facilities.
- Monitor clinical studies and ensure they are recorded and reported and meet SOPs, and applicable regulatory requirements.
- Help investigative sites with acquiring and maintaining IRB and EC approval.
- Request any updated site-related essential and non-essential documentation assess for content and ensure it complies with regulatory requirements.
- Ensure investigative sites report adverse happenings consistent with protocol specifications.
- Associate and / or Bachelor’s degree required.
- A minimum of 1 year clinical research experience in regulated medical device.
- Post market experience.
- Strong understanding of Good Clinical Practice (GCP).
- Experience in orthopedics desirable.
- CCRA or CCRP certification preferred.
- Experience with electronic data capture (EDC) technology an advantage.
Job Features
| Job Category | Pharmaceutical |
| Reference Number | FEB19KG |
We are excited to be recruiting for a global pharmaceutical company in their search for a Manager, Pricing Analytics and Reporting. Join a company that combines far-reaching and innovative therapeutic solutions that are helping to shape positive and meaningful change!
Awesome potential for career advancement and professional development!
Organization: Explore an opportunity to join a forward-thinking pharmaceutical company that combines breakthrough research and innovation while staying true to their values of integrity, quality, teamwork, and trust.
Culture: provides a collaborative work environment that empowers and enables their employees.
Position Focus:
- Develop analytical tools to gauge the influence of current and new US Federal and State Price Transparency laws with regard to the in-line portfolio and the late stage pipeline.
- Collaborate with Legal, Compliance, Brands and other stakeholders across all critical areas to infer the law in relation to price action calculations.
- Work alongside the Director of Pricing to determine key analytics that affect pricing strategy.
- Pinpoint any at-risk activities and their projected impact on the organizations ability adhere to US Federal and State Price Transparency Policies.
- A minimum of 5 years’ experience in the pharma/biotech industry; including 2+ years of pricing specific experience.
- Pricing and/or Market Access background, with experience developing pricing models and working on state legislation for transparency reporting.
- Knowledgeable re: Wholesale Acquisition Cost (WAC) pricing.
- Bachelor’s degree required; Master’s degree preferred.
Job Features
| Job Category | Pharmaceutical |
| Reference Number | FEB4C |
| Salary | $120,000 - $140,000 plus bonus |
We have a terrific opportunity for a Senior Manager, Medical Writing-Neurology/CNS, with expertise in regulatory writing, to join a global pharmaceutical company leading drug development in neuroscience by combining state-of-the-art research with treatment solutions that create a positive and meaningful impact.
Awesome potential for career advancement and professional development!
Organization: Explore an opportunity to join a forward-thinking pharmaceutical company that combines breakthrough research and innovation while staying true to their values of integrity, quality, teamwork, and trust.
Culture: provides a collaborative work environment that empowers and enables their employees.
Position Focus:
- Develop PCS, protocols, and protocol amendments, often functioning as the compound lead. Lead and contribute to the writing of marketing application submission documents.
- Provide direction to other medical writing on how to apply industry and medical writing best practices.
- Contribute to process improvement across functional areas.
- Collaborate with teams to form project specific metrics that adhere with standard project metrics.
- Bachelor’s degree in Life Sciences, English, or other related discipline; advanced degree preferred.
- 5+ years of medical writing experience with specialization in the regulatory space including writing for submissions, IBs, NDAs, Module 2 summaries, etc.
- Therapeutic experience in Neuroscience/CNS; with experience in epilepsy, movement disorders, and neurodegenerative diseases a plus.
- Certification in Medical Writing/Regulatory Writing (RAC) desirable.
Job Features
| Job Category | Pharmaceutical |
| Reference Number | FEB4B |
| Salary | $120,000 -$140,000 plus bonus |
Our client, a global pharmaceutical leader with a VERY robust oncology pipeline, is seeking a Director, Market Access Strategy, to manage the development and implementation of responsibility for Market Access Operations for 12+ distinctive indications, and 8+ different tumor types.
We are looking for a cross-functional leader with extensive experience in Market Access and Organized Customer Strategy to lead Oncology Market Access and be an integral part of collaborative efforts organization-wide.
Awesome potential for career advancement and professional development!
Organization: Explore an opportunity to join a forward-thinking pharmaceutical company that combines breakthrough research and innovation while staying true to their values of integrity, quality, teamwork, and trust.
Culture: provides a collaborative work environment that empowers and enables their employees.
Position Focus:
- Support market access strategy in Oncology through collaborating across all of market access including pricing, payer, reimbursement, and supplier relations.
- The main liaison with the organization’s alliance partner’s market access to develop launch plans on new indications, and market access resources.
- Oversee approval process for resources for the payer team and develop approaches for aligned and new products to ensure commercial success of the portfolio.
- Will really be responsible for determining market access strategy and leading work teams; developing ideas for pull through across various channels; will navigate IDNs, specialty pharma, large oncology clinics, etc.; and develop messaging and tools for field teams.
- Work alongside legal, compliance, and regulatory to understand existing and new interface / interaction with customers.
- Will engage with stakeholders including C-Suite executives, payers, physicians, specialty pharmacy, KOLs, PBMs, and policy and pathway development.
- 10+ years’ experience in the pharmaceutical industry with progressive responsibility and/ or diverse experience.
- Strong expertise in Market Access Strategy paired with Account Management experience.
- Knowledge of the competitive healthcare landscape and the payer customer’s decision cycle, with insight of how this affects decisions as well as the ability to transfer this knowledge into actionable insights in order to formulate strategies.
- Experience developing valid metrics, gathering information, and pinpointing potential opportunities to enhance new product planning, and strategy evolution.
- Bachelor’s degree in life sciences or business; advanced degree preferred.
Job Features
| Job Category | Pharmaceutical |
| Reference Number | FEB4A |
| Salary | Competitive compensation package includes generous base salary, bonus, LTI |