Top 266 Research associate ii, quality control Jobs in Boston, Ma

Clinical Research Associate II
AbbVie —Boston, MA
- $84,500 - $162,000 a year
- Full-time
- Remote
- Nursing
- Mid-level
- Organizational skills
- Paid holidays
- Health insurance
Research Associate II, Bioanalytical
Keros Therapeutics —Lexington, MA
- $62,000 - $87,000 a year
- Full-time
- Bachelor's degree
- Communication skills
- Entry level
Clinical Research Associate II/III - US
Optimapharm d.o.o. —Boston, MA
- $75,000 - $100,000 a year
- Full-time
- Remote
- Nursing
- Computer literacy
- Mid-level
- Dental insurance
- Paid time off
Research Associate II, CRISPR-X - LNP
CRISPR Therapeutics, Inc. —South Boston, MA
- $85,000 - $92,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
Quick Apply
Research Associate II, Quality Control
Ocular Therapeutix —Bedford, MA
- $85,000 - $93,000 a year
- Research
- Mid-level
- Bachelor's degree
Quality Control Analyst, II
Vericel Corporation —Burlington, MA
- $33.65 - $38.46 an hour
- Full-time
- Microsoft Word
- Microsoft Outlook
- Inventory management
Quick Apply
IN-PROCESS QUALITY INSPECTOR - 1st Shift
Primo Medical Group —West Bridgewater, MA
- $19 - $20 an hour
- Full-time
- Background check
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
11d
Quality Control Technician
Boston's Best Coffee Roasters —South Easton, MA
- From $18 an hour
- Full-time
- Spanish
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
4d
Mechanical Inspector for CNC Machine Shop (Watertown, MA)
Confidential-Manufacturing —Watertown, MA
- $60,000 - $80,000 a year
- Full-time
- Mid-level
- In-person
- 1 year
- Profit sharing
- Health insurance
Quick Apply
Sr. Quality Control Analyst
Pace Analytical Life Sciences —Waltham, MA
- $35 - $50 an hour
- Full-time
- English
- Master's degree
- Bachelor's degree
- Wellness program
- Health savings account
Manufacturing Data Coordinator
Hologic —Marlborough, MA
- $46,400 - $69,600 a year
- Full-time
- Oracle
- Mid-level
- 3 years
Quality Inspector III (B,C & D Shifts)
SRG —Acton, MA
- $35 - $40 an hour
- Night shift
- 5 years
- In-person
- Senior level
Quick Apply
Quality Control Technician
The Middlesex Corporation —Andover, MA
- Full-time
- Civil engineering
- Construction site
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
10d
Quality Control Technician- Aerospace (2nd Shift)
Poly6 —Burlington, MA
- $25 - $34 an hour
- Full-time
- Background check
- Pass drug screening
- English
- Paid holidays
- Health insurance
Manager-Quality Engineering
Microchip Technology —Lawrence, MA
- $91,000 - $247,000 a year
- Full-time
- 3 years
- Supervising experience
- Travel
- Employee stock purchase plan
- Health insurance
Concrete Quality Control Lead
Confidential —Abington, MA
- $30 - $35 an hour
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Health insurance
- Dental insurance
Quick Apply
Install Quality Control
Milltown Plumbing —Chelmsford, MA
- $30 - $50 an hour
- Full-time
- Clean driving record
- Mid-level
- Driving
- Paid training
- Paid holidays
Quick Apply
Senior Director, Quality Control
EPM Scientific —Boston, MA
- Contract
- Bachelor's degree
- Mentoring
- US work authorization
Quick Apply
3d
Quality Inspector Technician
Myomo, Inc —Burlington, MA
- $26 - $28 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Neurology
Quick Apply
2d
Manager Quality Control
TransMedics, Inc. —Andover, MA
- $118,600 - $148,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Engineering
- Employee stock purchase plan
- Disability insurance
Quick Apply

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Clinical Research Associate II

AbbVie -
Boston, MA

Apply Now

Job Details

Full-time
$84,500 - $162,000 a year

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

Stakeholder relationship building

Full Job Description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance.
Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.
Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.

Responsibilities

Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s positioning.
Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment principles for the trial ensuring a trusted partnership.
Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects.
Advanced understanding of site engagement and ability to customize site engagement strategy for assigned study (ies). Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy.
Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.
Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance.
Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development.
May participate in global/local task forces and initiatives. Responsible for activities as assigned by manager.
Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues.
Advanced ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution. Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a customer centric approach.
Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.
Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
Ensures audit and regulatory inspection readiness at assigned clinical site at all times.
Manages investigator payments as per executed contract obligations, as applicable.

Qualifications

Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred.
Minimum of 1 year of clinically related experience, of which a period of 6 months is required in clinical research monitoring of investigational drug or device trials. Familiar with risk‐based monitoring approach, onsite and offsite monitoring.
Knowledge of appropriate therapeutic area indications is preferred with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials.
Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.
Demonstrate strong cross-functional collaboration skills among internal and external stakeholders.
Demonstrate strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.
Advanced ability to leverage technology, tools and resources to provide customer centric support based on the health of the site.
Strong interpersonal skills with excellent written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training.
Ability to use functional expertise with appropriate guidance, leverage critical thinking skills and apply good judgement to address clinical site issues.
Acts with integrity in accordance with AbbVie code of business conduct and leadership values. Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role atthe time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors includinggeographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested,and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to aparticular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion,consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Apply Now

Refine Your Search

research associate ii, quality control jobs in boston, ma

Clinical Research Associate II

Research Associate II, Bioanalytical

Clinical Research Associate II/III - US

Research Associate II, CRISPR-X - LNP

Research Associate II, Quality Control

Quality Control Analyst, II

IN-PROCESS QUALITY INSPECTOR - 1st Shift

Quality Control Technician

Mechanical Inspector for CNC Machine Shop (Watertown, MA)

Sr. Quality Control Analyst

Manufacturing Data Coordinator

Quality Inspector III (B,C & D Shifts)

Quality Control Technician

Quality Control Technician- Aerospace (2nd Shift)

Manager-Quality Engineering

Concrete Quality Control Lead

Install Quality Control

Senior Director, Quality Control

Quality Inspector Technician

Manager Quality Control

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