Clinical Affairs Specialist

🔥 0 minutes ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $68.2k - $116k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

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Haemonetics

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1980

⚕️ Healthcare Insurance

💊 Pharmaceuticals

Healthcare Insurance • Pharmaceuticals

Haemonetics is a company that provides a suite of innovative medical technology solutions aimed at improving the quality, effectiveness, and efficiency of healthcare. The company focuses on optimizing operations for plasma centers, enhancing patient care in hospitals, and driving efficiency in blood centers by offering advanced technologies that improve productivity, quality, and safety. Haemonetics is committed to advancing healthcare standards and creating better outcomes for patients through their technology and services.

📋 Description

• Support day-to-day activities for one or more company sponsored clinical studies from planning and start-up through reporting and close-out under the direction of project leadership • Support development and maintenance of study plans, timelines, trackers, and operational documentation • Track study activities, site communications, and assigned deliverables to support execution against project timelines • Collaborate with internal stakeholders, CROs, vendors, and clinical sites to support study execution and ensure assigned activities are completed in accordance with protocols and applicable regulations (e.g., GCP, FDA, ISO 14155) • Support site and vendor interactions, including coordination of study materials, communications, follow-up items, and documentation needs • Escalate operational issues, delays, or risks to project leadership as appropriate • Maintain proper study documentation, including TMF maintenance • Draft and review key clinical documents such as ICFs, CRFs, tracking logs, operational plans, study plans, and IRB submissions • Support data review, data cleaning, query follow-up, reconciliation, and issue resolution activities in collaboration with data management, CROs, and study teams • Identify data discrepancies, protocol deviations, and documentation gaps and escalate issues appropriately • Support study and clinical regulatory activities including participation in study design, data review, protocol and report development, and contribution to clinical sections of regulatory submissions (e.g., IDE, PMA, 510(k), EU MDR) • Support audit and inspection readiness activities, including document preparation, follow-up, and resolution of assigned action items • Update company SOPs, templates, and protocols/reports for clinical requirements

🎯 Requirements

• Bachelor’s degree in life sciences or related field • 2+ years of experience in clinical affairs, clinical research, regulatory affairs, or a related field, preferably in the medical device industry • Strong understanding of GCP, ICH guidelines, and applicable regulatory requirements • Experience working with vendors, sites, and cross-functional teams • Excellent organizational, problem-solving, and communication skills • Ability to manage multiple priorities in a fast-paced environment • Strong attention to detail with emphasis on data quality, documentation accuracy, and reporting consistency • Basic understanding of clinical data analysis and issue resolution

🏖️ Benefits

• Health insurance • 401(k) with up to a 6% employer match and no vesting period • Employee stock purchase plan • Flexible time off for salaried employees • Accrual of three to five weeks’ vacation annually for hourly employees (based on tenure) • Accrual of up to 64 hours (annually) of paid sick time • Paid and/or floating holidays • Parental leave • Short- and long-term disability insurance • Tuition reimbursement • Health and welfare benefits