Top 30 Clinical trial management associate Jobs in Oceanside, Ca

Clinical Trial Management Associate
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $88,776 - $133,156 a year
- Remote
- HIPAA
- Mid-level
- Bachelor's degree
Quick Apply
3d
Clinical Program Supervisor
Olive Crest —San Diego, CA
- $90,000 - $93,000 a year
- Full-time
- LMFT
- Management
- Doctoral degree
- Paid jury duty
- Health savings account
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11d
Clinical Research Associate, Full Service
5PY IQVIA RDS Inc. —Carlsbad, CA
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Drug Safety Associate
Viking Therapeutics, Inc. —San Diego, CA
- $77,000 - $90,000 a year
- Nursing
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Assistant Clinical Research Coordinator - Psych
UC San Diego Health —San Diego, CA
- $36.31 - $58.41 an hour
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5d
Clinical Research Associate, Full Service
IQVIA —Carlsbad, CA
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
CRA 1, IQVIA Biotech
IQVIA —Carlsbad, CA
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Distribution Associate
Catalent —San Diego, CA
- $50,000 - $54,000 a year
- Email
- Forklift
- High school diploma or GED
- Ability to lift 50 pounds
- Paid holidays
- Health insurance
Business Intelligence Analyst - ACTRI - Hybrid
UC San Diego Health —San Diego, CA
- $43.39 - $79.69 an hour
- 8 hour shift
- Hybrid work
- Pass drug screening
- System design
- Mid-level
3d
CRA 2, Early Clinical Development
IQVIA —Carlsbad, CA
- $90,200 - $150,400 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Senior Clinical Research Associate, Sponsor Dedicated
IQVIA —Carlsbad, CA
- $74,500 - $197,500 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Associate Director, Development Quality Assurance
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $154,500 - $196,873 a year
- Hybrid work
- 5 years
- Writing skills
- Master's degree
Quick Apply
Director, Administrative Services
UC San Diego Health —San Diego, CA
- $43.39 - $79.69 an hour
- Monday to Friday
- Customer service
- 5 years
- Pass drug screening
Senior Research Associate, MEDSCH/EMERG MED SVC
UC San Diego Health —San Diego, CA
- $36.13 - $58.11 an hour
- 8 hour shift
- Background check
- Pass drug screening
- Surgery
Senior Clinical Research Associate, Sponsor Aligned, Oncology
IQVIA —Carlsbad, CA
- $71,900 - $189,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
Registered Nurse HUDVASH Case Manager
US Veterans Health Administration —San Diego, CA
- $103,980 - $188,494 a year
- Online Application
- Hybrid work
- Background check
- Nursing
- Doctoral degree
- Paid holidays
- Dental insurance
1d
Senior Specialist, Product Performance, Medical Affairs
Abbott Laboratories —Temecula, CA
- $99,300 - $198,700 a year
- Full-time
- Nursing
- Medicine
- 5 years
- Health insurance
- Tuition reimbursement
Associate Director, Clinical Development - Neurology
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $168,820 - $250,502 a year
- Hybrid work
- Medicine
- 5 years
- Doctor of Philosophy
Quick Apply
2d
Research Associate II - Manufacturing
Amprion —San Diego, CA
- $70,000 - $85,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Head of Clinical Operations
Kumquat Biosciences Inc —San Diego, CA
- $225,000 - $325,000 a year
- Nursing
- 11+ years
- Bachelor's degree
Quick Apply
12d

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Clinical Trial Management Associate

Ionis Pharmaceuticals, Inc. -
Carlsbad, CA

Quick Apply

Job Details

$88,776 - $133,156 a year
3 days ago

Qualifications

Pharmaceutical regulatory compliance
HIPAA
Employee relationship building
FDA 21 CFR Part 11
Information security
Health information security
ICH guidelines
Health information regulatory compliance
Productivity software
Clinical quality assurance standards
Delegation

Full Job Description

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We’re pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.

At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees.

With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.

We’re building on our rich history, and we believe our greatest achievements are ahead of us. If you’re passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!

CLINICAL TRIAL MANAGEMENT ASSOCIATE (CTMA)

SUMMARY:

The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to contribute towards the successful management and execution of clinical trials.

RESPONSIBILITIES:

Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and distributes management reports from internal tracking systems at requested intervals
Collaborates with the Clinical Trial Manager and/or the Clinical Project Lead on the development of certain study-specific plans and/or processes
Presents at team meetings as needed (i.e., Clinical Trial Team Meeting, Project Team Meeting, Investigator Meeting, project training, etc.)
Collects and reviews essential documents from Investigational sites
Supports TMF set-up, maintenance, ongoing quality review, and final reconciliation of study documents
Participates in study specific tasks such as Investigator identification, recruitment, collection of Investigator regulatory documents and site activation
Contributes to the development of the Monitoring Plan and assists with ensuring appropriate quality and timely monitoring of clinical sites
Assists in development of study materials, case report forms (CRFs), informed consent documents for clinical studies
Works with internal and external team members (i.e. Clinical Supplies, Toxicology PK, Regulatory Affairs, Clinical Data Management and CRO/Vendors) to deliver high quality trial execution
Prepares investigational site reference materials (i.e., screening/enrollment logs, Delegation of Site Responsibilities form, Site Monitoring Log, etc.)
Acts as primary contact for study contractors (e.g., contract CTMs, field CRAs)
Keeps the Clinical Project Lead (CPL) informed of the progress of projects
Develops and maintains good working relationships with Investigators and study staff
Assists in the organization and preparation of and participates in Investigator Meetings (as applicable)
Performs document tracking and signature/approval follow-up, where applicable, including Confidential Disclosure Agreements (CDAs), contracts, proposals, invoices, and other study documentation
Executes meeting logistics (e.g., schedule meetings, distribute meeting agendas and minutes), as needed
Ensures timely study entry and updates to ClinicalTrials.gov
Assists with design and preparation of study related materials for the training of internal and external staff
Participates in co-monitoring activities and oversight of CRO or contract CRAs for pre-study, initiation, routine monitoring, and closeout visits
Assists with the tracking and management of study specific budgets
Participates in development of departmental processes, SOPs, and initiatives
Assists with facilitating resolution of data queries and requests from Clinical Data Management
Travel is variable and estimated at 20%

COMPETENCIES IDENTIFIED FOR SUCCESS:

Ability to work in a team or independently as required
Effective written and verbal communication skills
Critically evaluates job tasks and the impact on overall trial management objectives
Sound problem-solving capabilities
Good judgment in triaging issues from internal and external customers
Effectively collaborates with Clinical Trial Team members
Outstanding organizational skills with the ability to multi-task and prioritize
Exceptional attention to detail
Proven flexibility and adaptability

REQUIREMENTS:

Bachelor’s Degree preferred
Minimum of two (2) years in clinical research or healthcare related industry, or equivalent combination of education and experience; site monitoring experience a plus
Experience in scientific discipline and multiple therapeutic areas preferred
Experience/training in the following areas: GxP Regulations, ICH Guidelines, Good Quality Practices, 21 CFR Part 11 and Computer Security (Part 11, Electronic Records; Electronic Signatures-Scope and Application; 21 CFR 11 and Industry Guidance; Computerized Systems Used in Clinical Trials), HIPAA, Drug Development and Approval Process
Proficiency in MS Office including Word, Excel, and PowerPoint

Please visit our website, http://www.ionis.com (http://www.ionis.com) for more information about Ionis and to apply for this position; reference requisition # IONIS004035

Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits (https://ionis.com/careers#:~:text=Highly%20competitive%20benefits)

Full Benefits Link: https://ionis.com/careers#:~:text=Highly%20competitive%20benefits (https://ionis.com/careers#:~:text=Highly%20competitive%20benefits)

The pay scale for this position is $88,776 to $133,156

NO PHONE CALLS PLEASE. PRINCIPALS ONLY.

Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.

#LI-Remote

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

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Refine Your Search

clinical trial management associate jobs in oceanside, ca

Clinical Trial Management Associate

Clinical Program Supervisor

Clinical Research Associate, Full Service

Drug Safety Associate

Assistant Clinical Research Coordinator - Psych

Clinical Research Associate, Full Service

CRA 1, IQVIA Biotech

Distribution Associate

Business Intelligence Analyst - ACTRI - Hybrid

CRA 2, Early Clinical Development

Senior Clinical Research Associate, Sponsor Dedicated

Associate Director, Development Quality Assurance

Director, Administrative Services

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Senior Specialist, Product Performance, Medical Affairs

Associate Director, Clinical Development - Neurology

Research Associate II - Manufacturing

Head of Clinical Operations

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