EP Clinical Manager – Orlando, FL – Boston Scientific – Orlando, FL
Company: Boston Scientific
Location: Orlando, FL
Expected salary:
Job date: Thu, 01 May 2025 22:54:16 GMT
Job description:
Job Description: Clinical Research and Technical Support Specialist
Position Summary:
We are seeking a dynamic Clinical Research and Technical Support Specialist to join our team. This role involves collaborating with various departments, including Clinical Research, Marketing, and Technical Support, to develop and implement optimal solutions that enhance our services and products. You will play a critical role in bridging communication between teams and ensuring that our clients receive the highest level of support.
Key Responsibilities:
- Collaborate with cross-functional teams to identify and implement innovative solutions in clinical research and product development.
- Provide ongoing training and support to internal staff and clients, ensuring comprehensive understanding of processes and technologies.
- Conduct assessments and analyze data to inform decision-making and improve operational efficiencies.
- Develop and maintain training materials, manuals, and resources for staff development.
- Serve as a point of contact for technical inquiries and provide expert advice and troubleshooting.
- Monitor industry trends and best practices, contributing to the continuous improvement of training programs.
Qualifications:
- Bachelor’s degree in a relevant field (Life Sciences, Marketing, or Technical Support preferred).
- Proven experience in clinical research, marketing, or technical support roles.
- Strong analytical skills and attention to detail.
- Excellent communication and interpersonal skills.
- Ability to work collaboratively in a team-oriented environment.
- Proficient in relevant software and tools.
If you are passionate about clinical research, innovative solutions, and training development, we invite you to apply and help us drive our mission forward!
EP Clinical Manager – Orlando, FL – Boston Scientific – Orlando, FL
Company: Boston Scientific
Location: Orlando, FL
Expected salary:
Job date: Fri, 02 May 2025 07:31:32 GMT
Job description:
Job Description: Clinical Research and Support Specialist
Position Summary:
We are seeking a dedicated Clinical Research and Support Specialist to join our dynamic team. In this role, you will collaborate across various departments—Clinical Research, Marketing, Technical Support, and more—to develop optimal solutions that enhance our services and product offerings.
Key Responsibilities:
- Collaborate with cross-functional teams to identify and analyze clinical research needs.
- Develop and implement strategies to optimize research protocols and improve outcomes.
- Provide ongoing training and development to team members and stakeholders.
- Assist in marketing initiatives by supplying clinical insights and data to bolster campaigns.
- Offer technical support and guidance to ensure smooth operation of clinical research initiatives.
- Monitor and evaluate project progress, ensuring compliance with regulatory requirements and internal standards.
Qualifications:
- Bachelor’s degree in a relevant field (Life Sciences, Marketing, etc.).
- Strong background in clinical research methodologies.
- Excellent communication and interpersonal skills.
- Proficiency in data analysis tools and software.
- Ability to work collaboratively in a fast-paced environment.
What We Offer:
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- A supportive and innovative work environment.
Join us in advancing clinical research and supporting effective solutions that make a difference!
Johnson & Johnson – Associate Scientific Director (Hematology) – Toronto, ON
Company: Johnson & Johnson
Location: Toronto, ON
Expected salary:
Job date: Thu, 10 Apr 2025 22:28:46 GMT
Job description: 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 https://www.jnj.comJob Function:
Medical Affairs GroupJob Sub Function:
Medical AffairsJob Category:
People LeaderAll Job Posting Locations:
Toronto, Ontario, CanadaJob Description:Our 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 Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.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 https://www.jnj.com/innovative-medicineThe Multiple Myeloma Associate Scientific Director, is responsible for medical and scientific leadership within the assigned therapeutic area to ensure seamless integration of inline and pipeline assets into the health care system. As a remote, head-office role, the Associate Scientific Director will lead Key Institution Management by implementing institution plans for key sites and networks within geographic regions, focusing on scientific, clinical, and evidence-generation activities. This role drives Medical Affairs strategy at assigned Canada institutions focusing on innovation and across portfolio-wide Hematology-Oncology activities. The Associate Scientific Director is responsible and accountable for providing high level, evidenced-based, scientific expertise to internal and external partners and stakeholders. This role plays a key strategic role in developing and advancing the scientific objectives of the organization. In collaboration with Field Managers, the Associate Scientific Director provides direction and guidance to the MSL Team on areas of interest to Janssen to develop and implement field-based activities aligned with the Medical Affairs Plan and Strategy.Responsibilities include but are not limited to:Lead the development of strategy for key institution management and implement institution plans for key sites and networks within assigned geographic regions that support the Hematology-Oncology pipeline of productsEstablish and maintain trusted peer-to-peer relationships with KOLs to collaborate on scientific projects, share balanced scientific data, collect insights and collaborate on future clinical research/publicationsDrive pre-launch and launch activities and strategic projects from Launch Readiness (LRT), Medical integration (MIT) and Patient Value Teams (PVT), as relevant to key institutionsLead and coordinate field engagement with key institutions focusing on medical and research initiatives, as well as strategic projects and partnershipsDevelop and maintain relationships with external opinion leaders/investigators involved in the delivery of care in Hematology-Oncology or engaged in related studiesProvide strategic input/direction to therapeutic MSLs/MSL Manager in the development and execution of their functionsProvide strategic scientific support to key stakeholders (marketing, access, regulatory) with respect to pipeline productsIdentify internal scientific training needs and collaborate with functional partners in its development and execution to ensure organizational readinessCollaborate with Medical Director and/or Therapeutic Area Head to build the pre-launch medical strategy, participate and co-lead NBD IEGP (As required) for all qualifying pipeline productsIn collaboration with the Therapeutic Area Head, identify and develop future clinical trial investigators and new trial sites to ensure quick adoption of new disease areas and technologiesQualifications – ExternalA minimum of a Doctoral degree is required; PhD, PharmD or MDMinimum of 5 years relevant therapeutic and/or pharmaceutical experience, strong clinical and/or scientific background and track record of collaboration in a matrix environmentPrior Hematology/Oncology experience is highly preferredExcellent written and verbal communication skills with both scientific and lay audiencesProven track record developing, presenting and publishing clinical or related evidence generation studiesStrong leadership skills and the ability to motivate teamsStrong planning and organizational skills: manage multiple projects concurrentlyDemonstration of a strong publication track recordAbility to work effectively in a matrix project team environment, partnered with strong project management and execution skills (proactive in identifying opportunities)Ability to critically review the medical literature and summarize the results for internal partnersExpert in navigating clinical or medical project approval systems, in statistical methods and processes for successful publicationAbility to (international & domestic) travel as required approximately 40%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.ERADICATE CANCER
Thermo Fisher Scientific – Field Service Engineer II (Toronto REMOTE) – Toronto, ON
Company: Thermo Fisher Scientific
Location: Toronto, ON
Expected salary:
Job date: Fri, 14 Mar 2025 23:51:17 GMT
Job description: Work Schedule Standard (Mon-Fri)Environmental Conditions Able to lift 40 lbs. without assistanceJob DescriptionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.Location/DivisionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.The Chemical Analysis Division (CAD) provides a broad mix of analytical instruments and services to a diverse range of end-user markets including Safety & Security, Environmental, Food Safety, Life Sciences, Medical, Energy, Spectroscopy and Minerals and Mining. Its instruments are used worldwide in various settings, both in the field and on the line, where customers value adaptability, reliability, and ease of use. CAD operates within a global footprint with more than 4,000 colleagues, delivering product solutions to customers that allow for confident, on-the-spot decision-making. CAD, part the Analytical Instruments group and is comprised of three business units:
- Measurement Control and Sample Identification
- Environmental and Process Monitoring
- Production Process and Analytics
- Bulk Elemental Analysis
The position supports the Bulk Elemental Analysis (BEA) business unit. This business drives value for our customers by enabling them to:
- accelerate production,
- improve product quality,
- make process decision faster,
- and protect their brands
We manufacture high-quality analytical, product inspection, bulk weighing, and compliance solutions and serve multiple sectors with a focus on:
- Clean Energy (battery manufacture & minerals production),
- Food Safety (Product inspection and food packaging), and
- Infrastructure (cement, mining & metals).
Product InspectionIn-line inspection and monitoring solutions to ensure safety, quality, and production efficiency by detecting physical contaminants, validating net content, verifying product integrity, and analyzing constituents. We supply systems worldwide to over 35,000 customers including the majority of the top 50 food companies. More… PGNAA & Minerals Processing Elemental AnalyzersWhen the world leaders in cement production, energy production (coal), and mining are concerned about the quality of the raw materials they process or consume, they call on Process AnalyticsImagingOur imaging product line of X-ray sources is crafted to provide accurate and consistent results for a variety of applications including high-resolution imaging and automated X-ray inspection on high-throughput production lines.Bulk Elemental Analysis (BEA)For more than 85 years, the Thermo Fisher Scientific Ecublens site in Switzerland has been a global supplier of spectrochemical instruments for major industries such as metallurgy, transportation, cement, mining, food, pharmaceuticals, chemicals, petroleum and batteries. We offer unparalleled capabilities in , and spectrometer automation (SMS).Discover Impactful Work:Territory: up to 75% travel in territory (Canada, Ontario Province)What will you do?You will provide complete services on Spectroscopy instruments: optical emission spectroscopy (OES), x-ray florescence (XRF), and x-ray diffraction (XRD) including installation, repairs, preventative maintenance, and instrument qualifications. In addition to working with our customers, you will also regularly engage with other team members, sales, technical support, and engineering.
- Perform on-site installation, repair, maintenance, qualification, and validation of
, systems. * Use customer management software to resolve service calls, control parts inventories, and complete job tasks.
- Inspect malfunctioning products, analyze inspection findings to detect the source of problem, and recommends repair, replacement, or other corrective action.
- Provide a communication link between the customer and the company to help ensure that effective service is provided to the customer.
- Develop and conduct training on the safe operations of the equipment and demonstrates skills to trainees, including both team members and customers.
Minium Education & Experience
- High school diploma and 4+ years hands-on experience as a Service Engineer and Technical Support Engineer, particularly working with analytical instrumentation. Working experience with
, is a strong plus or Bachelor’s degree in Sciences, Engineering or related field with 0 years’ experience.Proficiencies
- Customer oriented.
- Technical knowledge of scientific equipment or related technology based equipment.
- Effective interpersonal communication and ability to establish good customer rapport
- Ability to prioritize service requests and produce clear and concise documentation
- Ability to work independently within a customer location. Minimal direct supervision required.
Travel & Physical/Environmental requirements:
- Ability to travel up to 70% at times within the territory or other areas as needed.
- Physical activities: stooping, kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting, fingering, grasping, feeling, talking, hearing, repetitive motions.
- Ability to safely lift 50 Lbs. with assistance on occasion, and safely lift and carry 25-30 Lbs. continuously throughout the day.
- Environmental conditions: Inside office environment conditions, travel by taxi, train, airplane, noise, hazards, & conditions at customer locations.
- Maintain a valid driver’s license and safe driving record
BenefitsWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Intertek – Senior Scientific Consultant, Toxicology & Risk Assessment – Mississauga, ON – Mississauga, ON
Company: Intertek
Location: Mississauga, ON
Expected salary:
Job date: Fri, 04 Apr 2025 22:40:45 GMT
Job description: In this exciting, challenging, and fast-paced role, the successful candidate will exercise their scientific expertise and project management talents, work with our broader team of experienced toxicology and regulatory affairs experts, and use their industry contacts to grow and expand our consulting services. The Senior Scientific Consultant, Toxicology will lead and guide our clients on matters related to regulatory toxicology and compliance to global regulations and expectations for pharmaceuticals. This role requires a special individual with a deep understanding of, and appreciation for, toxicological risk assessments pertaining to drugs, biologics, and medical devices. Demonstrated expertise in the practices of sound scientific judgment and clear and transparent argumentation to support toxicological risk assessments in report formats that are regulatory-ready is indispensable. Experience in a breadth of projects involving different aspects of health-based exposure limits, occupational toxicology, and qualitative assessments will be critical, and an understanding of global regulatory expectations related to pharmaceuticals and safety is expected. An understanding of toxicology as related to safety testing programs in the formal development of new drugs, biologics, medical devices and other healthcare products would be beneficial. The Senior Scientific Consultant, Toxicology will directly engage with and support Intertek’s clients, serving as a representative of the consultancy and as a subject matter expert for toxicological risk assessments.Responsibilities:
- As a senior scientist, be responsible for work on and guidance of projects, which typically have major complexities and multiple dimensions/facets, identification of “out of the box” solutions when needed, and synthesis of findings into clear, well-written reports that discuss the implications of the findings. The Senior Scientific Consultant, Toxicology will be responsible for the quality and scientific accuracy of the final deliverable to the client, which may have included own work and that of colleagues/team and will need to meet project and Industry standards, regulatory requirements, and client expectations.
- Act as the primary liaison with Intertek clients, including initial business development meetings, through preparation of cost estimates for projects, formal project proposals and plans, and communication during the course of projects.
- Be an effective supervisor and team leader, responsible for a group or an area of expertise, who makes effective decisions about work to be done and work standards. Balance, or assist others in balancing, the needs of projects and resolving potential conflicts among competing projects or programs.
- Be a senior consultant, able to identify and capitalize on business development opportunities. Attract a flow of work from new and existing clients based on own reputation and expertise in the field. Have a good understanding of the work of the company as a whole, including an understanding of local and global trends, and help plan and support the growth and development of the business accordingly.
- Act as a senior leader for the team: support leadership in meeting goals and objectives and contribute to the development of junior staff.
Desired Qualifications:
- PhD in Toxicology (preferred) or related field, or MSc or other related degree or training.
- 10 years of pharmaceutical industry experience with a primary focus on toxicology, and more specifically toxicological risk assessments.
- Subject matter expertise: scientific acumen in toxicological risk assessments, understanding of the role of regulatory toxicology and pharmaceutical safety, ability to solve complex scientific problems, and experience guiding clients with their project or program needs.
- Demonstrated consulting skills: business acumen to identify project needs and encourage additional client work requests; experienced at the preparation of accurate cost and timeline estimates. Operating at a very high level of professional standards and integrity to ensure project parameters and standards are met at all times.
- Excellent communicator and manager, able to practice effective time management, and able to manage complex projects. Enjoys working within a team including more senior and more junior team members.
- Excellent communication skills in both verbal and written format; able to develop persuasive, clear arguments and rationales.
Personal Characteristics:
- Well organized and structured, with a keen attention to detail.
- Excellent customer service and interaction skills.
- Enjoys the challenge of analyzing and solving problems.
- Able to self-motivate to meet project or submission timelines, process information, and work independently in a fast-paced, multi-tasking environment, but also a team player able to contribute work on a number of different parts of a project.
- Able to work in a hybrid environment, ideally split between remote work (home-based) and in the office in Mississauga, Ontario, Canada.
Salary & Benefits InformationWhen working with Intertek, you can expect salary and benefit package competitively placed within the local market, including medical, dental, vision, life, disability, Registered Retirement Savings Plan (RRSP) with company match, generous vacation/sick time (PTO), tuition reimbursement and more. Intertek employees are eligible for a variety of benefits including paid holidays.Intertek’s CommitmentIntertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers’ expectations, while engaging with our employees to be 10X in their performance and professional growth.Our Culture of Total Quality AssuranceIntertek promotes a culture where motivated, customer-oriented employees can flourish, experience professional fulfillment, and reach their highest potential. At Intertek, we exercise our spirit of innovation, the passion of our people and our unmatched customer commitment to realize our purpose of making the world an ever better, safer, and more sustainable place for all.A career with Intertek offers rewarding opportunities to help companies around the world develop products that are used safely by millions of people every day. Intertek is the trusted advisor to many of the world’s leading brands, companies, and governments, and has earned a reputation for accuracy, reliability, integrity, and technical competence. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.We Value DiversityIntertek’s network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.For individuals with Disabilities, who would like to request accommodation, or who need assistance applying, please email hr.canada@intertek.comPlease apply online at Intertek Canada Careers (oraclecloud.com)*Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume.
Intertek – Senior Scientific Consultant, Toxicology & Risk Assessment – Mississauga, ON – Mississauga, ON
Company: Intertek
Location: Mississauga, ON
Expected salary:
Job date: Fri, 04 Apr 2025 22:15:52 GMT
Job description: In this exciting, challenging, and fast-paced role, the successful candidate will exercise their scientific expertise and project management talents, work with our broader team of experienced toxicology and regulatory affairs experts, and use their industry contacts to grow and expand our consulting services. The Senior Scientific Consultant, Toxicology will lead and guide our clients on matters related to regulatory toxicology and compliance to global regulations and expectations for pharmaceuticals. This role requires a special individual with a deep understanding of, and appreciation for, toxicological risk assessments pertaining to drugs, biologics, and medical devices. Demonstrated expertise in the practices of sound scientific judgment and clear and transparent argumentation to support toxicological risk assessments in report formats that are regulatory-ready is indispensable. Experience in a breadth of projects involving different aspects of health-based exposure limits, occupational toxicology, and qualitative assessments will be critical, and an understanding of global regulatory expectations related to pharmaceuticals and safety is expected. An understanding of toxicology as related to safety testing programs in the formal development of new drugs, biologics, medical devices and other healthcare products would be beneficial. The Senior Scientific Consultant, Toxicology will directly engage with and support Intertek’s clients, serving as a representative of the consultancy and as a subject matter expert for toxicological risk assessments.Responsibilities:
- As a senior scientist, be responsible for work on and guidance of projects, which typically have major complexities and multiple dimensions/facets, identification of “out of the box” solutions when needed, and synthesis of findings into clear, well-written reports that discuss the implications of the findings. The Senior Scientific Consultant, Toxicology will be responsible for the quality and scientific accuracy of the final deliverable to the client, which may have included own work and that of colleagues/team and will need to meet project and Industry standards, regulatory requirements, and client expectations.
- Act as the primary liaison with Intertek clients, including initial business development meetings, through preparation of cost estimates for projects, formal project proposals and plans, and communication during the course of projects.
- Be an effective supervisor and team leader, responsible for a group or an area of expertise, who makes effective decisions about work to be done and work standards. Balance, or assist others in balancing, the needs of projects and resolving potential conflicts among competing projects or programs.
- Be a senior consultant, able to identify and capitalize on business development opportunities. Attract a flow of work from new and existing clients based on own reputation and expertise in the field. Have a good understanding of the work of the company as a whole, including an understanding of local and global trends, and help plan and support the growth and development of the business accordingly.
- Act as a senior leader for the team: support leadership in meeting goals and objectives and contribute to the development of junior staff.
Desired Qualifications:
- PhD in Toxicology (preferred) or related field, or MSc or other related degree or training.
- 10 years of pharmaceutical industry experience with a primary focus on toxicology, and more specifically toxicological risk assessments.
- Subject matter expertise: scientific acumen in toxicological risk assessments, understanding of the role of regulatory toxicology and pharmaceutical safety, ability to solve complex scientific problems, and experience guiding clients with their project or program needs.
- Demonstrated consulting skills: business acumen to identify project needs and encourage additional client work requests; experienced at the preparation of accurate cost and timeline estimates. Operating at a very high level of professional standards and integrity to ensure project parameters and standards are met at all times.
- Excellent communicator and manager, able to practice effective time management, and able to manage complex projects. Enjoys working within a team including more senior and more junior team members.
- Excellent communication skills in both verbal and written format; able to develop persuasive, clear arguments and rationales.
Personal Characteristics:
- Well organized and structured, with a keen attention to detail.
- Excellent customer service and interaction skills.
- Enjoys the challenge of analyzing and solving problems.
- Able to self-motivate to meet project or submission timelines, process information, and work independently in a fast-paced, multi-tasking environment, but also a team player able to contribute work on a number of different parts of a project.
- Able to work in a hybrid environment, ideally split between remote work (home-based) and in the office in Mississauga, Ontario, Canada.
Salary & Benefits InformationWhen working with Intertek, you can expect salary and benefit package competitively placed within the local market, including medical, dental, vision, life, disability, Registered Retirement Savings Plan (RRSP) with company match, generous vacation/sick time (PTO), tuition reimbursement and more. Intertek employees are eligible for a variety of benefits including paid holidays.Intertek’s CommitmentIntertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers’ expectations, while engaging with our employees to be 10X in their performance and professional growth.Our Culture of Total Quality AssuranceIntertek promotes a culture where motivated, customer-oriented employees can flourish, experience professional fulfillment, and reach their highest potential. At Intertek, we exercise our spirit of innovation, the passion of our people and our unmatched customer commitment to realize our purpose of making the world an ever better, safer, and more sustainable place for all.A career with Intertek offers rewarding opportunities to help companies around the world develop products that are used safely by millions of people every day. Intertek is the trusted advisor to many of the world’s leading brands, companies, and governments, and has earned a reputation for accuracy, reliability, integrity, and technical competence. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.We Value DiversityIntertek’s network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.For individuals with Disabilities, who would like to request accommodation, or who need assistance applying, please email hr.canada@intertek.comPlease apply online at Intertek Canada Careers (oraclecloud.com)*Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume.
Scientific Inside Sales Specialist – Danaher – Vancouver, BC
AF Solutions Clinical Specialist II – Orlando, FL – Boston Scientific – Orlando, FL
Company: Boston Scientific
Location: Orlando, FL
Expected salary: $65000 – 85000 per year
Job date: Sat, 15 Mar 2025 23:29:41 GMT
Job description: The job involves collaborating with various departments within the WATCHMAN organization, such as sales, clinical research, marketing, technical, training, and strategic planning, to develop creative and feasible solutions. The role also includes assisting management in recruiting and coaching team members. Strong communication and teamwork skills are essential for this position in order to effectively work with related personnel and contribute to the overall success of the organization.
AF Solutions Clinical Specialist II – Orlando, FL – Boston Scientific – Orlando, FL
Company: Boston Scientific
Location: Orlando, FL
Expected salary: $65000 – 85000 per year
Job date: Sun, 16 Mar 2025 05:07:39 GMT
Job description: The ideal candidate for this position will be responsible for generating creative and feasible solutions for various projects within the organization. This will involve collaborating with different departments such as sales, clinical research, marketing, and technical teams to ensure smooth implementation of strategies. Additionally, the individual will work closely with key stakeholders across the organization including Marketing, Training, and Strategic Planning to achieve common goals. The candidate will also be expected to support management in recruiting and coaching team members to drive success and innovation within the company. Strong communication and leadership skills are essential for this role.