Top 7054 Program associate Jobs in Boston, Ma

Clinical Trial Associate
CRISPR Therapeutics, Inc. —South Boston, MA
- $85,000 - $95,000 a year
- Full-time
- Bachelor of Science
- Quality control
- SharePoint
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11d
Senior Associate in Tax, Assurance & Advisory Services
D.J. Gustafson & Co., CPA P.C. —East Weymouth, MA
- $46 - $62 an hour
- Full-time
- Hybrid work
- CPA
- Office
- Senior level
- Health insurance
- Dental insurance
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5d
Quality Assurance Associate - Day & Employment
Charles River Center —Needham, MA
- $31.25 an hour
- Full-time
- English
- Mid-level
- 3 years
Quality Assurance Associate - Residential
Charles River Center —Needham, MA
- $31.25 an hour
- Full-time
- English
- Mid-level
- Residential
Associate Attorney
King, Tilden, McEttrick & Brink, (MI) PLLC —Braintree, MA
- $82,000 - $90,000 a year
- Email
- Analysis skills
- In-person
- 1 year
- AD&D insurance
- Disability insurance
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12d
Associate Executive Director - Corporate Compliance Officer
North Charles Mental Health Research and Training Foundation, Inc —Cambridge, MA
- $73,000 - $80,000 a year
- Full-time
- HIPAA
- Office
- Master's degree
- Health savings account
- Health insurance
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Associate / Lead Dentist - $10k Sign-On Bonus
Tend —Cambridge, MA
- $175,000 - $425,000 a year
- Email
- CPR Certification
- Dental office
- Management
- Wellness program
- Commuter assistance
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Associate General Dentist
Dentmax —Lynn, MA
- $150,000 - $300,000 a year
- Part-time
- Anatomy knowledge
- Dental office
- HIPAA
- Professional development assistance
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Case Worker Manager | Transitional Age Youth Program
The Home for Little Wanderers, Inc. —Dorchester, MA
- On call
- Computer literacy
- Mid-level
- Bachelor's degree
- 403(b) matching
- AD&D insurance
Samaritans Training Coordinator
Family Services of the Merrimack Valley —Lawrence, MA
- $20 - $22 an hour
- Weekends as needed
- Microsoft Excel
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
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Food Coordinator
Fox Hill Village —Westwood, MA
- $22 an hour
- Temporary
- Background check
- Microsoft Excel
- Microsoft Outlook
- 401(k)
- Paid time off
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Associate Director, Global Regulatory Affairs - Ad / Promo
BioNTech AG —Cambridge, MA
- $168,100 - $268,700 a year
- Full-time
- Background check
- Bachelor's degree
- Training & development
- Health savings account
- AD&D insurance
Claims Associate - Auto Property Damage
Plymouth Rock Assurance Corporation —Boston, MA
- $50,000 - $55,000 a year
- Office
- Bachelor's degree
- 1 year
- Wellness program
- Commuter assistance
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Lead Instructor Coordinator
Action Ambulance Service Inc —Wilmington, MA
- Classroom
- Mid-level
- Bachelor's degree
Quick Apply
Program Manager
Community Resources For Justice —Medway, MA
- Weekends as needed
- Bilingual
- Microsoft Outlook
- Writing skills
Quick Apply
13d
Development Coordinator
USS Constitution Museum —Charlestown, MA
- Weekends as needed
- Hybrid work
- Research
- Mid-level
- Bachelor's degree
- 403(b) matching
- Health insurance
Quick Apply
Mental Health Intensive Care Coordinator - Master's Level
The Home for Little Wanderers, Inc. —Dorchester, MA
- Full-time
- Spanish
- Computer literacy
- Mid-level
- 403(b) matching
- AD&D insurance
Sales Support Coordinator - Grocery
HWY Partners —Natick, MA
- $50,000 - $65,000 a year
- Full-time
- Microsoft Outlook
- Merchandising
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Retail Sales Associate-Wrentham Village Premium Out
Bath & Body Works —Wrentham, MA
- $16.50 an hour
- Part-time
- Merchandising
- Ability to lift 50 pounds
- Fair chance
- Store discount
- Paid parental leave
Medical Billing Coordinator
New England Podiatry Associates —Chestnut Hill, MA
- From $25 an hour
- Full-time
- Research
- Mid-level
- In-person
- Health insurance
- Dental insurance
Quick Apply

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program associate jobs near boston, ma

Clinical Trial Associate

CRISPR Therapeutics, Inc. -
South Boston, MA

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Job Details

Full-time
$85,000 - $95,000 a year
11 days ago

Qualifications

Presentation software
Document control experience within pharmaceutical industry
Filing
Cross-functional collaboration
Clinical trial support in drug product development
Achieving project delivery timelines
Pharmaceutical research experience
Cross-functional communication

Full Job Description

Job Description:

Company Overview

Founded over a decade ago, CRISPR Therapeutics is a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY® (exagamglogene autotemcel [exa-cel]), the world’s first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. CRISPR Therapeutics is advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase™ editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact, CRISPR Therapeutics has established strategic collaborations with leading biopharmaceutical partners, including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California.

Position Summary

Working closely with the Clinical Trial Manager, the Clinical Trial Associate (CTA) position will assist with daily clinical trial execution activities including the coordination of documents associated with the conduct of investigational clinical studies in accordance with applicable regulations, Good Clinical Practice (GCP), and CRISPR Therapeutics standard operating procedures (SOPs). The ideal candidate will have keen attention to detail and has the ability both to prioritize and independently handle multiple tasks effectively.

This incredible opportunity will put the right candidate at the forefront of medicine, working on ground breaking trials with tremendous potential to impact patient's lives. You will join a team of incredibly dedicated professionals whose talent is matched by their commitment and passion for the work we are doing. A team that remains focused on what's important for the patient and also has an incredible track record of growth and development among them. If you are looking to learn, work hard, and make a difference, we would like to speak with you.

Responsibilities

Help maintain tracking systems and tools to support the conduct of a clinical study from start-up to close-out
Collect trial information and disseminate it to the internal project team, the CRO, and other stakeholders
Coordinate study meetings, materials and agendas; recording and disseminating decisions and actions
Responsible for internal meeting agendas/minutes as applicable
Responsible for updating, maintaining and quality control of the eTMF, SharePoint site and shared drive
Responsible for study laboratory sample tracking and vendor management support
Coordinate version control of clinical documents, prioritize multiple tasks and/or projects
Assist in coordination and tracking of clinical supply shipments, including review and approval of Regulatory Greenlight Documentation Packages
Support Clinical Operations team in new process development or optimization
Effectively communicate with study team members and work closely to address challenges

Minimum Qualifications

BS/BA degree or equivalent and at least 1-3+ years experience in clinical research
Knowledge of drug development, clinical operation processes and documentation including study start up procedures, maintenance phase, and study close out procedures
Knowledge and implementation of the processes involved in clinical studies following Good Clinical Practice (GCP) and the Code of Federal Regulations
Experience with eTMF; ability to directly apply essential document knowledge to file documents
Effective communication, organizational and interpersonal/team skills
Proficient in MS Excel, Word and PowerPoint.
Established ability to prioritize and manage multiple tasks simultaneously, demonstrated ability to identify and resolve issues, and effectively manage timelines
Participate in inter-departmental workgroups to create or enhance processes
Strong attention to quality/detail
Good organizational and time management skills
Willingness to work in a flexible environment

Preferred Qualifications

Experience inside a Sponsor or CRO company
Experience with global studies, using an outsourced CRO model
Experience in clinical drug development with knowledge of First in Human trials
Experience with regulatory affairs, including IND/CTA submissions

Competencies

Collaborative – Openness, One Team
Undaunted – Fearless, Can-do attitude
Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
Entrepreneurial Spirit – Proactive. Ownership mindset.

CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.

Base pay range of $85,000 to $95,000+ bonus, equity and benefits

The range provided is CRISPR Therapeutics’ reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.

CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.

To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy

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Refine Your Search

program associate jobs in boston, ma

Clinical Trial Associate

Senior Associate in Tax, Assurance & Advisory Services

Quality Assurance Associate - Day & Employment

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Associate Attorney

Associate Executive Director - Corporate Compliance Officer

Associate / Lead Dentist - $10k Sign-On Bonus

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Case Worker Manager | Transitional Age Youth Program

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Food Coordinator

Associate Director, Global Regulatory Affairs - Ad / Promo

Claims Associate - Auto Property Damage

Lead Instructor Coordinator

Program Manager

Development Coordinator

Mental Health Intensive Care Coordinator - Master's Level

Sales Support Coordinator - Grocery

Retail Sales Associate-Wrentham Village Premium Out

Medical Billing Coordinator

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