The Opportunity That Awaits You: The Clinical Associate Representative will provide technical and clinical support for the AQUABEAM Robotic System and provide surgeon and staff training, in-service support, and clinical assistance for existing and potential customers. This role may also be responsible for field service support including system installations and repairs and making software upgrades. At the core of this role, we are looking for an individual with the ability to manage very complex surgical procedures and sophisticated robotically assisted operations in the operating room. This requires a high level of management, attention to detail, and the ability to orchestrate multiple professionals all at once. The Clinical Associate Representative will also work to create competency, comfort, and expertise with all PROCEPT BIOROBOTICS technologies among physicians and support staff. The ideal candidate works well in a team environment and can exercise independent judgment in planning, organizing, and performing their work. The role will also work closely with various Procept teams on system modifications or execution of any field-based requirements specific to the AQUABEAM Robotic System.
What Your Day-To-Day Will Involve:
- Provides medical professionals with product training, support, information, and training on the use of Company products and with staff education, in-services, and technical troubleshooting.
- Works closely with the Clinical Specialist, Professional Education and Sales & Marketing team to design, develop and facilitate training for sites and internal and external customers.
- Ensures Professional Education programs run efficiently, are effective and compliant to our regulatory standards.
- Provides instruction to surgeons and participants in formal classroom and field settings.
- Troubleshoots product issues in the field and respond to staff and customer product issues.
- Supports the team to ensure presentations are consistent with PROCEPT BioRobotics' goals and objectives and in compliance with PROCEPT BioRobotics' indications for use.
- Provides customer feedback to Marketing on product design and customer utilization needs.
- Builds a strong clinical background and understanding with the ability to support Surgeons and Healthcare Professionals.
- Maintain trained status for, and comply with, all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance.
- Understand and adhere to the PROCEPT BioRobotics Quality & EHS policies.
The Qualifications We Need You to Possess
- Bachelor's degree from accredited reputable institution
- 1 – 2 years of sales experience preferred
- Ability to travel upwards to 75% (primarily domestic)
- Solid knowledge in science and medical devices industry
- Computer proficiency in Microsoft Office
- Outstanding communication skills (clear and concise in all forms of communications)
- Ability to function effectively across many departments
- Maintain strong attention to detail
- Ability to handle multiple assignments and effectively adapt or change priorities as needed
- Creative problem-solving skills and the willingness to take calculated risks and act decisively (but should communicate potential consequences to enable informed business decisions)
- Ability and willingness to "roll up the sleeves" and become actively engaged in tactical execution
- Ability to extract and position key data elements from clinical studies that support safety and effectiveness in a concise, compelling manner
- Excellent interpersonal and presentation skills with the ability to persuade in a credible fashion
EQUAL EMPLOYMENT OPPORTUNITY STATEMENT PROCEPT BioRobotics is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind on the basis of race, color, national origin, religion, gender, gender identity, sexual orientation, disability, genetic information, pregnancy, age, or any other protected status set forth in federal, state, or local laws. This policy applies to all employment practices within our organization. PAY RANGE TRANSPARENCY Procept is committed to fair and equitable compensation practices. The pay range(s) for this role represents a base salary range for non-commissionable roles or on-target earnings for commissionable roles. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, relevant certifications and training, and specific work location. Based on the factors above, Procept utilizes the full width of the range. The total compensation package for this position may also include eligibility for annual performance bonus, equity, and the benefits listed above. WORK ENVIRONMENT We'll provide you training for, and ask you to maintain trained status for, and comply with, all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance. We would also ask you to understand and adhere to the PROCEPT BioRobotics Quality & EHS policies. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
-
Tokyo Intuitive ¥3,000,000 - ¥9,000,000 per yearダビンチサージカルシステムの稼働率を最大化する責務を担い、各地域の市場に合わせたコンサルティング型の営業活動を実施し、新製品の紹介や消耗品等の販売を行う。 · 主要な手術手技におけるダビンチ手術の専門家として、手術チームの「パートナー」としての地位を確立する。 · ...
-
Tokyo Hays臨床研究サイトおよび臨床試験参加に関する患者データおよび研究関連情報を監視します。調査員が研究プロトコル、規制要件、良好な臨床慣行に従い、データ検証計画への入力を提供します。患者データのタイムリーかつ正確なモニタリングと、ソースドキュメント、研究記録、およびサイト訪問から、必要に応じて調査関連情報を提供します。 · 臨床試験を実施する能力を評価するために、潜在的なサイトのサイト選択を実施します。 · サイト開始訪問を実行し、サイトのスタッフがすべての試験関連の側面に完全に訓練されていることを確認します · さまざまな問題を解決するための会社の方針と手順を ...
-
Tokyo Hays臨床研究サイトおよび臨床試験参加に関する患者データおよび研究関連情報を監視します。調査員が研究プロトコル、規制要件、良好な臨床慣行に従い、データ検証計画への入力を提供します。患者データのタイムリーかつ正確なモニタリングと、ソースドキュメント、研究記録、およびサイト訪問から、必要に応じて調査関連情報を提供します。 · 調査サイトおよび監査施設の選択を監視します。 · 臨床試験を実施する能力を評価するために、潜在的なサイトのサイト選択を実施します。 · さまざまな問題を解決するための会社の方針と手順を適用します。 · コスト センターの目標と目標に貢献します ...
-
Japan PROCEPT BioRobotics ¥9,000,000 - ¥12,000,000 per yearThe Clinical Associate Representative will provide technical and clinical support for the AQUABEAM Robotic System and provide surgeon and staff training, in-service support, and clinical assistance for existing and potential customers. · Provides medical professionals with produc ...
-
Japan Heidi ¥4,000,000 - ¥12,000,000 per yearAs a Growth Associate at Heidi Health, you are empowered to establish and scale Heidi Health's presence in Asia, out of Japan from the ground up. You are responsible for developing a leading and sustainable market position - not by following a predefined playbook, but by creating ...
-
Tokyo ICON plc ¥420,000 - ¥840,000 per yearClinical Site Associate in Tokyo Osaka - Office Hybrid at ICON plc, a world-leading healthcare intelligence and clinical research organization. · ...
-
Tokyo Heidi ¥800,000 - ¥2,000,000 per year+Job summary · A Clinical Growth Associate at Heidi Health will establish and scale Heidi Health's presence in Asia from scratch. · +ResponsibilitiesOwning the success of Heidi Health across Asia. · Developing market leadership through full-cycle execution. · ...
-
Tokyo Sandoz ¥3,000,000 - ¥6,000,000 per yearThis job involves reviewing and evaluating non-clinical data, planning clinical development strategy, and executing bioequivalence studies. · Review and evaluate non-clinical/clinical data · Plan clinical development strategy with assistance from manager and global team · ...
-
Japan BeiGene ¥6,000,000 - ¥12,000,000 per yearWe are seeking a Clinical Research Associate II/Senior Clinical Research Associate to join our team. As a key member of our organization, you will be responsible for executing clinical trial protocols at clinical trial sites and monitoring clinical trials by ICH guidelines and GC ...
-
Minato Novartis ¥4,000,000 - ¥6,000,000 per yearClinical Research Associate monitors patient data and research-related information at clinical research sites and clinical trials. Investigator provides input to data validation plans in accordance with research protocols, regulatory requirements, and good clinical practices. Pro ...
-
Tokyo Dell Technologies ¥2,500,000 - ¥6,000,000 per yearJoin us as an Associate Inside Sales Representative on our Sales team in Tokyo to do the best work of your career and make a profound social impact. · Be immersed in the sales and technology industry by talking to and building relationships with customers as well as qualifying op ...
-
Tokyo Fortrea Full time¥3,600,000 - ¥6,000,000 per yearThe Clinical Research Associate II will be responsible for site management, conducting site monitoring responsibilities, and preparing project plans related to clinical monitoring. The ideal candidate will have a thorough understanding of ICH GCP Guidelines and local regulatory r ...
-
Minato Novartis ¥2,500,000 - ¥5,000,000 per yearMonitor patient data and research-related information for clinical research sites and clinical trials. Provide input to data validation plans and offer investigation-related information as needed from source documents, research records, and site visits. Monitor the selection of i ...
-
Japan, Tokyo IRE ¥520,000 - ¥1,168,000 per yearClinical Site Associate role at ICON plc in Tokyo Osaka with office hybrid setup. ...
-
Japan, Tokyo IRE ¥500,000 - ¥1,200,000 per yearClinical Site Associate - Office Hybrid role at ICON plc in Tokyo Osaka, fostering an inclusive environment driving innovation and excellence. · Competitive salary and benefits package. · Diverse culture that rewards high performance and nurtures talent. · ...
-
Tokyo Sandoz ¥8,000,000 - ¥14,000,000 per year+Execute bioequivalence studies pharmacodynamic studies clinical endpoint studies healthy subjects patients accordance GCP regulatory requirements assistance Manager Vender Management documents PMDA consultation collaboration local regulatory affairs global team prepare submissio ...
-
Minato NovartisWe are seeking an Associate Clinical Sciences Trial Leader to lead or support global cross-functional clinical trial teams in the early clinical development stage (Phase 1 to Phase 2a). · Lead or support the creation of clinical trial implementation plans in collaboration with Me ...
-
Tokyo, Tokyo Deep Intelligent Pharma ¥1,800,000 - ¥2,500,000 per yearDeep Intelligent Pharma is pioneering the transformation of the pharmaceutical industry with a revolutionary AI-native, multi-agent platform. Our mission is to empower pharmaceutical and medtech innovators by turning regulatory and clinical complexity into a catalyst for speed, s ...
-
Minato Novartis ¥10,000,000 - ¥20,000,000 per yearThe Japan Program Clinical Head (JPCH) is responsible for clinical program activities for approval and post approval commitment for Re-examination in Japan. · Lead the JCT and represent Clinical Development on the JPT to achieve valuable clinical program strategy, drive innovatio ...
-
Ebisu, Tokyo Teva Pharmaceuticals ¥2,000,000 - ¥2,500,000 per yearAssociate Director, Clinical Project Management - Japan is responsible to plan, lead and oversee the operational execution of Teva's clinical programs in Japan across all indications from Phase I to Phase IV, in terms of cost, quality, timeliness and efficiency, while assuring pa ...
-
Japan - Tokyo Gilead Sciences ¥5,000,000 - ¥15,000,000 per yearWe are seeking an Associate Director, Clinical Development to play a key role in the scientific planning, execution and reporting of Japanese clinical studies for Gilead's development compounds in inflammation and virology therapeutic area. · ...