Title: Clinical Annotator Location: East Coast United States Job Description: Role - Clinical Subject Matter Expert & Data Abstractor Location - Remote Job Summary We are seeking a highly skilled and detail-oriented Clinical Subject Matter Expert (SME) to lead clinical pre-annotation validation and data abstraction. This role is critical for our incremental annotation process, focusing on the human validation of NLP-generated data and the precise abstraction of clinical elements from complex medical records. The successful candidate will bridge the gap between raw clinical documentation and high-quality structured datasets, specifically supporting studies in neurology (ICH and Seizures). Key Responsibilities - Clinical Data Abstraction: Perform deep-dive reviews of clinical notes for cohorts of up to 150 patients with Intracerebral Hemorrhage (ICH) and 150 patients with new-onset seizures. - Targeted Data Extraction: Assess and extract up to 18 specific data elements (5-9 per outcome) across patient groups as defined by client protocols. - Dataset Management: Accurately enter abstraction findings into patient-specific datasets and ensure timely delivery of high-quality data to the client. Clinical Annotators to abstract facts from notes and update those in CRFs - Annotation Validation: Perform rigorous human validation on pre-annotated data generated by commercial NLP models (e.g., Amazon Comprehend Medical) or internal LLM tools. - Guideline Refinement: Contribute to the iterative improvement of annotation guidelines to enhance inter-annotator agreement and resolve disagreements between model outputs and human validation. - Cross-functional Collaboration: Partner with Data Science and NLP teams to provide feedback on model performance and assist in the creation of "golden datasets" for model evaluation. - Compliance: Maintain strict adherence to HIPAA, data privacy, and security protocols regarding sensitive US patient data. Qualifications Must-Have (Required): - Education: Bachelor's or Master's degree in a Healthcare/Life Sciences field (e.g., Nursing/RN, BAMS, BHMS, Pharmacy, or Clinical Research). - Experience: Proven experience in Clinical Data Abstraction or medical record review. - Clinical Competency: Strong ability to interpret unstructured US clinical documentation (Discharge Summaries, Physician Progress Notes, Imaging Reports). - Technical Proficiency: Solid understanding of NLP concepts and experience with data annotation tools (e.g., Label Studio, Prodigy, Inception). - Detail Oriented: Exceptional accuracy in identifying minute clinical data elements across 100+ page patient files. Good-to-Have (Preferred): - JSL Expertise: Prior experience within the John Snow Labs (JSL) ecosystem, specifically Health AI Lab and GenAI tools. - Therapeutic Knowledge: Specific experience in Neurology (Stroke/ICH/Seizures) or Oncology (ECOG/Karnofsky scores). - Advanced Annotation: Experience with Named Entity Recognition (NER), Relationship Extraction, and Assertion Status. - Process Knowledge: Familiarity with incremental batch training and machine learning lifecycles. Work Environment This job operates in a professional office environment. This role routinely uses standard office equipment, including but not limited to, computers, phones, and photocopiers. Physical Demands This position requires the frequent and repetitive use of a computer, keyboard, and mouse. Hand and finger dexterity is required. EEO Saama provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws

Role Description Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site start-up. Prepare, distribute and follow-up on start-up documents with sites. Plan and track site start-up activities and data using designated systems and tools. Provide reports on intelligence and metrics related to study start-up activities. - Please note there is 1 position cross-posted in several locations, although we are open to considering candidates from the following countries: Poland, UK, Romania, Germany. Site Start-Up Packages - In cooperation with Project Management create study-specific start-up document package. - Distribute and follow up with sites to obtain the required executed documents. - Review content and correctness of returned documents from the sites, in accordance with internal standards. - In conjunction with Regulatory Affairs, ensure that the correct and complete packages are obtained within the planned timelines. Site Contract and Budget Negotiation - In co-operation with Contract and Legal, obtain feedback on suggested site and investigator contract language. - Act as main point of contact for sites to obtain feedback on budget and contract negotiations. - In conjunction with the Project Manager, provide sites with the suggested study budget and negotiate within pre-approved margins. Site Intelligence Tracking - Maintain site intelligence tracker with data related to specific requirements for study sites such as start-up timelines, budget, contract negotiation timelines and prerequisites, patient recruitment data, etc. - Provide input for suggested site list during start-up using past experiences with potential study sites. Site Start-Up Planning and Tracking & Project Management support - Act as main contact for study sites during start-up. - Develop and maintain relationships with study sites that will facilitate timely completion of start-up. - In conjunction with project management and CRAs, plan start-up actions and provide expected SIV dates for individual sites based on previous start-up metrics, as well as regulatory and RB timelines. - Track progress of start-up activities in smart sheet and/or CTMS. - Maintain up to date knowledge, ensure adherence and compliance with local regulatory requirements and associated documentations. - Provide support to project management with study related activities as required. Qualifications - Minimum of one to three years of related work experience with ongoing training, or a minimum of a one-year College Advance Diploma/Degree in a relevant field of study, preferable in Health or Life Sciences, or Clinical Research. - Excellent communication skills. - Knowledge of start-up requirements for clinical sites. - Experience in working directly with clinical study sites through previous involvement in studies. - Very high sense of urgency. Working Conditions - Home-based. Additional Information - PHISHING SCAM WARNING: Alimentiv is aware of the continued increase of phishing scams, leveraging various methods of attack via email, text, voice and social media. Please note that Alimentiv only uses company email addresses, which contain “@alimentiv.com”, to communicate with candidates via email. - If you are contacted by someone about an open job at Alimentiv, please verify the domain of the sender’s email address and that they are asking you to apply on this website. - If you believe you’ve been a victim of a phishing scam, please contact your local government cyber authority to report. - Accommodations for job applicants with disabilities are available upon request. - 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.

Description The Senior Medical Science Liaison (MSL) Oncology will build and maintain relationships with key oncology healthcare providers and decision-makers in the thoracic oncology space. The candidate will deliver presentations and engage in strategic discussions on Catalyst’s products and disease states of interest, covering medical, clinical, health economics, and outcomes of research data. They will interact with a wide range of healthcare professionals, including physicians, researchers, and medical and pharmacy leaders. This includes engagement with hospital and formulary decision-makers, Medicaid stakeholders, advocacy leadership, consultant pharmacists, and advanced practice practitioners. This is a remote position and will cover the EAST region. Candidates should reside within the east region and have access to major airports on the east coast. Requirements Responsibilities included but not limited to: - Identify, develop, and maintain collaborative relationships with current and future key external experts (KOLs), scientific experts, cooperative study groups and study sites - Collaborate with key professionals at the national, regional, and local level, educating them with current, fair-balanced medical, scientific and pharmacoeconomic information regarding Catalyst’s various therapies and disease states of interest - Increase awareness of our marketed product(s) allowing the key healthcare professionals to make informed therapeutic decisions - Assist in the preparation and execution of regional and/or national advisory board meetings for marketed and pipeline assets, including delivering compelling presentations, assisting with slide preparation/review, recommending appropriate faculty, and facilitating interactive discussion groups - Offer resources for presenting medical information, enabling feedback from decision makers on the effectiveness of our product and its market comparison - Provide targeted internal training on selected topics in oncology and supportive care (e.g., study updates, guideline updates, congress news, latest scientific developments); implement and disseminate high-quality medical and scientific educational programs; deliver clinical and scientific presentations at sites/hospitals - Facilitate Catalyst-sponsored clinical trials on-site through scientific presentations and discussions to build interest and provide study design feedback; understand trial/referral networks, identify enrollment barriers, and participate in investigator meetings per approved strategy - Expedite the development and collection of quality data for pipeline assets and our marketed product - Manage oncology-related projects from start to finish as directed by the medical affairs director - Contribute clinical and value-based insights to Catalyst communications and materials, and assist in training new associates, including medical science liaisons and regional account managers - Review and coordinate oncology-based investigator-initiated research, quality improvement initiatives, and screening/clinical pathway updates in the oncology space as it relates to Catalyst products Education/Experience/Skills: - Advanced degree in medical/biosciences (M.D., Ph.D., Pharm.D., DPH, Ed.D.) - 5+ years in clinical research/academia, pharmacy, life sciences, biotech or pharma industry (including relevant fellowships) - 3+ years of MSL experience in Oncology and Rare Disease, with a focus on medical affairs - Established relationships in the thoracic oncology therapeutic area - Knowledge of the pharmaceutical corporate environment and appreciation for Commercial Operations, including Marketing and Sales strategies - Strong scientific and pharmaceutical knowledge, with excellent presentation and teaching skills - Excellent written and verbal communication skills; confident in discussing drug information and disease state management - Willingness to work cross-functionally and compliantly within the organization - Ability to lead and motivate team members without direct reporting relationships, including training and mentoring new MSLs - Proven ability to assess issues and think strategically Description of Work: - Frequent Computer laptop or tablet use, not usually at a workstation - Responsibilities may require a work schedule that may include working outside of ‘normal’ work hours, to meet the demands of the organizations. (Advisory Boards, Congress Attendance, and other weekend type business activities) - Ability and willingness to travel at least 75% of workdays for face-to-face meetings required in the assigned geography with potential support needed throughout the US Catalyst is committed to providing competitive wages and comprehensive benefits including health, dental, and vision insurance, generous paid time off, a retirement savings plan with Company Match, and more. Further details about our benefits package can be found here: https://www.linkedin.com/company/catalystforrare/life/life-at-catalyst/?viewAsMember=true The base salary for this position will range from $208,000 to $225,000. Candidate experience, professional licensing, and geographic location will be taken into consideration. EEO Statement Catalyst Pharmaceuticals is an Equal Opportunity Employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status. Recruitment & Staffing Agencies: Catalyst Pharmaceuticals does not accept unsolicited agency resumes. Agency resumes will only be accepted if the agency is formally engaged by Catalyst Human Resources.

Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About the role: Boston Scientific was recognized as a “Glassdoor Best Place to Work” in 2026, ranking No. 15 on the Top 100 list. Boston Scientific’s Peripheral Vascular Associate is a transitional role designed to prepare candidates to become a Sales Consultant within the Vascular Therapies Division. The Peripheral Vascular Associate is assigned by region to an existing territory with opportunity to convert and grow the business. Peripheral Vascular Associates are accountable for delivering exceptional service through team-driven execution, revenue impact, clinical education support and identification of new business opportunities aligned with company strategy and priorities. This role works collaboratively with the Regional Sales Manager and territory Sales Consultant to support accounts and drive sales revenue. Each Peripheral Vascular Associate reports directly to a Regional Sales Manager. Additionally, Peripheral Vascular Associates may be required to support business needs outside of their primary territory assignments as business conditions require. At Boston Scientific, our products and technologies diagnose and treat a wide range of medical conditions within the venous system, including deep vein thrombosis, post-thrombotic syndrome, pulmonary embolism and compressive diseases. We continue to innovate in key areas and expand into new geographies and high-growth adjacency markets. Our solutions include AngioJet, Zelante DVT, thrombectomy catheters, EKOS, peripheral guidewires, drug-eluting stents and balloons, atherectomy and IVUS. We maintain a robust product pipeline and continue investing in interventional treatments that positively impact patient lives. Work model, sponsorship, relocation: This role follows a remote work model, allowing employees to work from a home-based location within the assigned region. Candidates must reside within the designated territory or be willing to relocate at their own expense. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time. Your responsibilities will include: • Build strong customer relationships through routine visits, product demonstrations, educational programs, product in-services, procedural observation and issue resolution • Develop relationships with physicians, nurses, technicians, materials management, nuclear medicine, hospital administration and infection control stakeholders • Provide procedural support in competitive clinical environments • Partner seamlessly with the Sales Consultant to increase selling time and drive account growth • Support revenue-generating projects and territory goals to strengthen account ownership • Collaborate with Sales Consultants and Regional Sales Managers to evaluate business conditions and sales trends • Assist in developing quarterly and annual business plans to achieve revenue targets • Provide timely updates to the Regional Sales Manager regarding business activities, competitive conditions and industry trends • Manage expense and promotional budgets within established guidelines • Maintain Sales Representative Assigned Inventory (SRAI) • Complete all required training within designated timelines • Execute quarterly and off-cycle inventory counts • Maintain accurate sales records and secure purchase orders • Submit administrative documentation in a timely manner • Conduct all sales activities in accordance with Travel and Entertainment guidelines, Advanced Policies and Integrity Policies • Participate in occasional weekend coverage, trade shows, internal meetings and other business-related travel, with travel expectations of 30% to 40% Required qualifications: • Bachelor’s degree in business, life sciences or related field, or equivalent experience in healthcare or a related industry • Minimum of 2 years' experience in sales, clinical support, healthcare or other relevant business environment • Documented record of achieving or exceeding performance goals • Demonstrated ability to build and maintain professional relationships with physicians, clinicians and hospital stakeholders • Proven ability to work independently while collaborating effectively within a team-based selling environment • Strong business acumen with the ability to analyze sales trends and contribute to territory planning • Demonstrated leadership potential with a proactive, solution-oriented approach • Ability to manage multiple priorities in a fast-paced, competitive environment • Willingness to travel 30% to 40% as required by business needs Requisition ID: 626555 The anticipated annualized base amount or range for this full time position will be $60,000, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs. For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability. Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn. Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code § 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination. Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.