UNKNOWN

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Essential Job Duties:Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes . The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.

<h3>Description</h3><br/><div>Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. <br/><br/>The <strong>Principal Investigator </strong>conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.</div><br/><h3>Key Responsibilities</h3><br/><div><strong>Essential Job Duties:</strong></div><ul><li>Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes </li><li>Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance</li><li>Evaluates and assesses participants to ensure only eligible participants enroll into the trials.</li><li>Participates and engages in successful delivery and retention of study participants.</li><li>Interacts positively and collaboratively with sponsors, clients and team members.</li><li>Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.</li><li>Actively involved in protocol training for staff.</li><li>Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.</li><li>Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.</li></ul><div><br/></div><br/><h3>Skills, Knowledge and Expertise</h3><br/><div><strong>Minimum Qualifications:</strong>  MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required.  Clinical Research experience is a plus. Board certification in area of specialty is required. CPR required / ACLS preferred.<br/><br/></div><div><strong>Required Skills: </strong></div><ul><li>Clinical skills and clinical procedures based in area of specialty. </li><li>Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm). </li><li>Must possess strong organizational skills, attention to detail, and math proficiency.</li><li>Well-developed written and verbal communication skills.  Bi-lingual (English / Spanish) proficiency is highly preferred.</li><li>Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.  </li><li>Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.</li><li>Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.</li><li>Must possess a high degree of urgency, self-motivation, integrity and dependability.</li><li>Ability to work independently to identify problems and implement solutions. </li><li>Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.</li></ul><div><br/></div><br/><h3>Benefits</h3><br/><ul><li>Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. </li><li>Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.</li></ul>

Alcanza Clinical Research

Clinical Research Physician - (Bilingual required - English/Spanish)

Clinical Monitoring

Clinical Research

Clinical Trial

Clinical Trial Management

Communication Skills

Corporate Policies

Dermatology

Detail Oriented

English Language

FDA (Food and Drug Administration)

GCP (Good Clinical Practices)

HIPAA (Health Insurance Portability and Accountability Act)

ICH Regulations

Identify Issues

Interpersonal Skills

Leadership

Mathematics

Medicine

Multilingual

Multitasking

National Institutes of Health (NIH)

Neurology

Organizational Skills

Patient Safety

Physician Credential

Presentation/Verbal Skills

Psychiatry and Mental Health

Regulations

Regulatory Compliance

Research Protocols

Spanish Language

Staff Training

Writing Skills

PinpointHQ

YEAR

Support virtual and in-person meetings with Forest Service leadership and staff. Provide real-time interpretation (English ↔ Spanish) during meetings and events.

<p style="text-align:center"><strong>English–Spanish Interpreter / Translator</strong></p><p><strong>Location:</strong> Puerto Rico (On-site and Virtual)<br/><strong>Client:</strong> USDA Forest Service – El Yunque National Forest<br/><strong>Type:</strong> Contract / On-Call</p><h2><strong>Key Responsibilities:</strong></h2><ul><li><p>Provide <strong>real-time interpretation (English ↔ Spanish)</strong> during meetings and events.</p></li><li><p>Support <strong>virtual and in-person meetings</strong> with Forest Service leadership and staff.</p></li><li><p>Ensure accurate translation of information while maintaining tone and intent.</p></li><li><p>Conduct brief <strong>pre-meeting coordination calls</strong> with agency staff when required.</p></li><li><p>Maintain confidentiality and comply with federal agency requirements.</p></li></ul><h2><strong>Qualifications:</strong></h2><ul><li><p><strong>Fluent in English and Spanish (spoken and written).</strong></p></li><li><p>Minimum <strong>3 years of interpretation or translation experience</strong>.</p></li><li><p>Knowledge of <strong>Puerto Rican culture and context</strong>.</p></li><li><p>Ability to support <strong>on-site and virtual meetings across Puerto Rico</strong>.</p></li></ul><p>Powered by JazzHR</p>

Ladgov Corporation

English–Spanish Interpreter / Translator

Data Quality

Federal Government

On Call

Plan Meetings

Translation Services

United States Department of Agriculture (USDA)

partner JazzHR

Overseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget). Collaborating with other departments (Business Development, Patient Recruitment, Finance, Budgets and Contracts, and Quality) to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors.

<h3>Description</h3><br/><div>Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. <br/><br/>The <strong>Manager, Clinical Operations </strong>is responsible for leading the operational performance of the clinical research staff. Provides on-site oversight to help ensure execution and coordination of clinical research activities according to ICH guidelines, GCP, FDA guidelines and follows company policies and procedures.</div><br/><h3>Key Responsibilities</h3><br/><div><strong>Essential Job Duties:</strong></div><ul><li>Overall team management and leadership support with a focus on driving study performance, enhancing efficiencies, patient safety and protocol/GCP/regulatory compliance.</li><li>Collaborating with other departments (Business Development, Patient Recruitment, Finance, Budgets and Contracts, and Quality) to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors.</li><li>Reviewing the performance dashboards and other clinical trial systems to oversee site and patient activities, ensure proper staff coverage, and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency).</li><li>Overseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget).</li><li>Assisting with initial and ongoing trainings regarding protocol specificities, Case Report Form (CRF) completion, Standard Operating Procedures (SOPs), clinical plans and guidelines, and timelines for the study.</li><li>Ensuring adherence to standard operating procedures, good clinical practice (GCP), FDA regulations, and company policies and procedures.</li><li>Overseeing site staff assigned to the study and routinely assessing study-specific process and training compliance, CMP compliance, and identifies emerging risks. May develop and support execution of corrective action plans at site and study level.</li><li>Overseeing people management activities including timecards, absence tracking/approvals, new hire training, interviewing and selection, performance appraisals, job description preparation, employee counseling, career coaching and employment meetings.</li><li>Managing assigned site staff, proactively identify and resolve issues, and work to ensure successful site operations.</li><li>Collaborating with investigators to ensure patient safety and meeting client goals and timelines.</li><li>Employing strategic thinking and problem-solving skills to propose and implement risk mitigations.</li><li>Participating and presenting in management or site meetings.</li><li>Perform all other duties as required or assigned.</li></ul><br/><h3>Skills, Knowledge and Expertise</h3><br/><div><strong>Minimum Qualifications:</strong><br/>Bachelor’s degree and a minimum of 2 years of clinical research experience, or an equivalent combination of education and experience, is required. 2+ years’ experience as a clinical research coordinator (CRC). 1+ years of management experience in clinical research is highly preferred. Bi-lingual (English / Spanish) proficiency is a plus.<br/><br/></div><div><strong>Required Skills:</strong></div><ul><li>Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).</li><li>Must possess strong organizational, time management, problem solving, and project management skills to meet project deadlines.</li><li>Well-developed written and verbal communication skills.</li><li>Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.</li><li>Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.</li><li>Must be professional, respectful of others, self-motivated, and have a strong work ethic.</li><li>Must possess a high degree of integrity and dependability.</li><li>Ability to work under minimal supervision, identify problems and implement solutions.</li><li>Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.</li></ul><br/><h3>Benefits</h3><br/><ul><li>Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. </li><li>Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.</li></ul>

Clinical Research Operations Manager - Bilingual required (English/Spanish)

Budgeting

Business Development

Career Counseling

Case Report Form (CRF)

Clinical Information Systems

Clinical Practices/Protocols

Corrective Action

FDA Requirements

Finance

Maintain Compliance

Operations Management

People Management

Performance Analysis

Performance Reviews

Problem Solving Skills

Procedure Implementation

Project/Program Management

Records Management

Reporting Dashboards

Risk Analysis

Risk Management

Standard Operating Procedures (SOP)

Team Lead/Manager

Time Management

PART_TIME

Location: USDA Forest Service, International Institute of Tropical Forestry (IITF), San Juan, Puerto Rico. Bimonthly: Deliver reports for the Forest Service American Relief Act 60-day Congressional Report.

<p><strong>Position:</strong> Scientific Writer <br/><strong>Location:</strong> USDA Forest Service, International Institute of Tropical Forestry (IITF), San Juan, Puerto Rico<br/><strong>Schedule:</strong></p><ul><li><p><strong>Monthly:</strong> Develop scientific briefings, blogs, research highlights, and outreach products.</p></li><li><p><strong>Quarterly:</strong> Submit written progress reports.</p></li><li><p><strong>Bimonthly:</strong> Deliver reports for the Forest Service American Relief Act 60-day Congressional Report.</p></li><li><p><strong>Annually:</strong> Provide text for an IITF Accomplishment Report.</p></li></ul><h3><strong>Key Responsibilities</strong></h3><ul><li><p>Translate technical and scientific findings into clear reports, articles, and outreach products.</p></li><li><p>Develop communication materials related to hurricane recovery and forest resilience science.</p></li><li><p>Provide writing support for briefings to USDA leadership, Congress, and the public.</p></li><li><p>Collaborate with IITF scientists and communication staff to consolidate evidence, photos, and project materials.</p></li><li><p>Advise on communication strategies for science delivery and branding.</p></li><li><p>Attend regular meetings to review deliverables and progress.</p></li></ul><h3><strong>Qualifications</strong></h3><ul><li><p>Master’s degree in communications, science writing, or related field.</p></li><li><p>At least 5 years of experience in scientific writing, public affairs, or communications.</p></li><li><p>Bilingual proficiency in English and Spanish.</p></li><li><p>Experience in public relations, outreach campaigns, and science branding.</p></li><li><p>Strong teamwork and collaboration skills in a research environment.</p></li></ul><p>Powered by JazzHR</p>

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English Jobs in San Juan, PR

Clinical Research Physician - (Bilingual required - English/Spanish) Alcanza Clinical Research

English–Spanish Interpreter / Translator Ladgov Corporation

Clinical Research Operations Manager - Bilingual required (English/Spanish) Alcanza Clinical Research

Scientific Writer Ladgov Corporation

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