Top 98 Scientist Jobs in Juncos, Pr

Early Phase Clinical Trials Manager
PanOncology Trials —Humacao Municipio, PR
- Full-time
- Spanish
- Nursing
- Medicine
- Health insurance
- Paid time off
Quick Apply
Applied Scientist - AI Trainer
DataAnnotation —San Juan, PR
- $50 - $100 an hour
- Part-time
- Remote
- Computer Science
- English
- Mid-level
- Flexible schedule
Quick Apply
Clinical Research Coordinator
PanOncology Trials —Humacao, PR
- Full-time
- Spanish
- Nursing
- Medicine
- Health insurance
- Paid time off
Quick Apply
Process Development Sr Scientist
Weil Group, Inc —Juncos, PR
- Temporary
- Background check
- Spanish
- Medicine
Quick Apply
Sr Data Engineer - Scientist
Kelly Services —Juncos, PR
- $48 an hour
- Full-time
- Spanish
- Computer science
- Computer Science
- Paid holidays
- Disability insurance
Quick Apply
8d
Technician-QC Laboratory
Eli Lilly —Carolina, PR
- $12.98 - $29.09 an hour
- Full-time
- Bachelor's degree
- US work authorization
- Manufacturing
- Health insurance
- Dental insurance
3d
Microbiologist
EB Validation Services —Caguas, PR
- Full-time
- Maintenance
- Bachelor's degree
- In-person
Quick Apply
Process Development Scientist
Cencora —Juncos, PR
- Full-time
- Spanish
- Word processing
- Computer literacy
- Paid parental leave
- Health insurance
Microbiologist - I
Galephar Pharmaceutical Research —Humacao Municipio, PR
- $15 an hour
- Full-time
- Background check
- Analysis skills
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
6d
Scientist II
BD —Cayey Municipio, PR
- Spanish
- Bachelor of Science
- Writing skills
Process Development Scientist
ECHO Consulting Group —Municipio de Juncos, PR
- Contract
- Spanish
- Doctoral degree
- Computer literacy
Quick Apply
6d
Medical Data Entry Specialist
PanOncology Trials —San Juan, PR
- Full-time
- Spanish
- English
- Administrative experience
- Health insurance
- Dental insurance
Quick Apply
CRA 2/Senior CRA 1
Lifelancer —San Juan, PR
- $76,300 - $175,100 a year
- Full-time
- Spanish
- Nursing
- English
Quality Control Scientist, Laboratory Chemist
Validation & Engineering Group —Municipio de Juncos, PR
- Spanish
- Management
- Doctoral degree
Quick Apply
Process Development Scientist 35588
ProQualityNetwork —Juncos, PR
- 12 hour shift
- Hybrid work
- Spanish
- Microsoft Excel
- Doctoral degree
Scientist 2 - Biology/Microbiology
PRPDG —Gurabo, PR
- $15 - $20 an hour
- Full-time
- Data analysis skills
- Mid-level
- Analysis skills
Quick Apply
12d
CRA 2/Senior CRA 1
IQVIA —San Juan, PR
- $76,300 - $175,100 a year
- Full-time
- Spanish
- Nursing
- English
Scientist III
BD —Cayey Municipio, PR
- Spanish
- 5 years
- Bachelor of Science
1d
Clinical Research Coordinator
Pan American Center for Oncology Trials LLC —San Juan, PR
- Spanish
- Nursing
- Medicine
Quick Apply
Research Assistant (Fixed Term Contract)
Puerto Rico Science Technology & Research Trust —San Juan, PR
- Full-time
- Spanish
- Microsoft Excel
- English
Quick Apply
10d

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scientist jobs near juncos, pr

Early Phase Clinical Trials Manager

PanOncology Trials -
Humacao Municipio, PR

Quick Apply

Job Details

Full-time

Benefits

Health insurance
Paid time off
Life insurance

Qualifications

Spanish
Clinical research
Interpersonal skills
English
Bachelor's degree
Attention to detail
Organizational skills

Full Job Description

We are seeking an Early Phase Clinical Trials Manager to lead the planning, coordination, and execution of early phase oncology clinical trials. The ideal candidate will have strong experience in clinical research, project management, regulatory compliance, and operational leadership, with the ability to manage multiple studies while ensuring high-quality study conduct, participant safety, and compliance with sponsor and regulatory requirements.

Responsibilities

Lead the planning, coordination, and execution of early phase oncology clinical trials from study start-up through study close-out.
Oversee study timelines, resources, logistics, and operational activities to ensure protocols are conducted in accordance with sponsor expectations, regulatory requirements, ethical standards, and institutional policies.
Coordinate study start-up activities, including site readiness, regulatory documentation, study activation, and operational planning.
Oversee patient recruitment, screening, enrollment, and informed consent processes to ensure protocol compliance and enrollment objectives are achieved.
Monitor study progress and proactively identify and resolve operational issues that may impact study timelines or quality.
Collaborate closely with Principal Investigators, Sub-Investigators, research nurses, clinical research coordinators, sponsors, CROs, study monitors, and other external partners to ensure successful study execution.
Support participant safety monitoring by ensuring timely reporting and documentation of adverse events and protocol deviations, as applicable.
Oversee the collection, review, and quality of clinical trial data while ensuring accurate and timely documentation in accordance with study protocols.
Maintain complete, organized, and audit-ready regulatory, source, and study documentation.
Coordinate sponsor monitoring visits, site qualification visits, audits, inspections, and regulatory reviews.
Oversee study supplies, investigational product accountability, and other site logistics necessary to support trial operations.
Prepare study reports, operational updates, and trial documentation for investigators, sponsors, and leadership.
Promote continuous improvement initiatives that enhance clinical operations, study efficiency, regulatory compliance, and the overall participant experience.
Provide leadership, guidance, and operational support to clinical research staff while fostering a collaborative and patient-centered research environment.

Qualifications

Bachelor's degree in Nursing (RN) or Medical Laboratory Technology (Lab Tech) required. Candidates holding a Medical Doctor (MD) degree or currently pursuing an MD are also encouraged to apply.
Experience in clinical research, preferably in oncology and/or early phase clinical trials, is highly desirable.
Strong project management skills with the ability to coordinate multiple studies, timelines, and operational priorities.
Experience coordinating study start-up activities, patient recruitment, informed consent, and clinical trial operations.
Knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and other applicable regulatory requirements.
Experience preparing for sponsor visits, audits, inspections, and regulatory reviews.
Familiarity with Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC) systems, and other clinical research technologies.
Strong organizational, leadership, communication, and problem-solving skills.
Ability to collaborate effectively with investigators, research nurses, clinical research coordinators, sponsors, CROs, and multidisciplinary teams.
Bilingual (English and Spanish).

We are an equal opportunity employer.

Job Type: Full-time

Benefits:

Health insurance
Life insurance
Paid time off

Experience:

Clinical research: 1 year (Required)

Language:

English (Required)

Work Location: In person

Quick Apply

Refine Your Search

scientist jobs in juncos, pr

Early Phase Clinical Trials Manager

Applied Scientist - AI Trainer

Clinical Research Coordinator

Process Development Sr Scientist

Sr Data Engineer - Scientist

Technician-QC Laboratory

Microbiologist

Process Development Scientist

Microbiologist - I

Scientist II

Process Development Scientist

Medical Data Entry Specialist

CRA 2/Senior CRA 1

Quality Control Scientist, Laboratory Chemist

Process Development Scientist 35588

Scientist 2 - Biology/Microbiology

CRA 2/Senior CRA 1

Scientist III

Clinical Research Coordinator

Research Assistant (Fixed Term Contract)

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