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Added 1 min ago
Technical Associate II
WEG Electric Corp
Duluth, GA
This role is responsible to perform technical research functions to support inside and outside sales personnel, with a focus on troubleshooting technical requirements presented by customers.
Added 2 mins ago
Assistant Director, Building Planning and Operations
Harvard University
Cambridge, MA
Monitors campus spaces and building aesthetics to support visual consistency, functionality, quality,
Added 3 mins ago
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Electronics Technician Work Study - Boston, MA
Lutron Electronics Co., Inc
Boston, MA
- $24 to $25 USD / hour
…work environment. Work studies are integrated directly into engineering teams and assigned meaningful real-world assignments. You may aid in the development and production of the next…
Added 3 mins ago
Electronics Technician Work Study - Coopersburg, PA
Lutron Electronics Co., Inc
Coopersburg, PA
…work environment. Work studies are integrated directly into engineering teams and assigned meaningful real-world assignments. You may aid in the development and production of the next…
Added 3 mins ago
Associate Field Service Technician
Toshiba Global Commerce Solutions - External
Topeka, KS
The Associate Field Service Technician is responsible for maintaining retail store technologies, computer systems and peripherals, within retail store and commercial business environments.…
Added 4 mins ago
Creative Services Consultant
Securian Financial Group
Saint Paul, MN
Designs and produces professional PowerPoint presentations and presentation templates that support marketing initiatives and business communications.
Added 5 mins ago
Instructor of Industrial Engineering
University of South Carolina
SC
The Department of Informatics and Engineering Systems at the University of South Carolina Upstate invites applications for a full-time, 9-month Instructor of Industrial Engineering,…
Added 6 mins ago
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Contract Conformance Specialist
Randstad USA
Houston, TX
- $37.03 to $48.44 USD / hour
Bachelor's degree with 6-10+ years of experience, or Associate degree with 10+ years of experience in legal, engineering, construction, or contract administration of construction projects…
Added 8 mins ago
Construction Manager - Electrical
IREN
Sweetwater, TX
Job Type: Full-time | Location: Sweetwater, Texas | Department: Construction | Reporting to: Associate Director, Construction | Work Location: #onsiteIREN is a vertically integrated AI…
Added 8 mins ago
Electrical Equipment Technician T1/T2 (Central Region)
Dominion Energy
RICHMOND, VA · MIDLOTHIAN, VA
…maintenance, testing, and commissioning of electrical equipment in support of Dominion Energy’s field facilities. Individuals in this role will build the foundational knowledge, skills, and…
Added 9 mins ago
Engineering Technician
HUSCO International, Inc.
Waukesha, WI
As an Engineering Technician with Husco, you’ll be at the heart of cutting-edge design and development- working side-by-side with our Design teams to bring bold ideas and customer solutions…
Added 9 mins ago
Associate Director, Facilities & Maintenance
Fujifilm
Research Triangle Park, NC
The Associate Director, Facilities & Maintenance leads multi-site or large-campus facilities operations, maintenance, and reliability programs to ensure safe, compliant, and cost-effective…
Added 10 mins ago
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Food Production Associate-2nd shift
E.A. Sween Company
Eden Prairie, MN
- $19 USD / hour
Adhere to all GMPs, standard work, and safety practices. Report any non-compliance to the Pack-off Lead or Support Supervisor.
Added 10 mins ago
Flex Associate-2nd Shift SC
E.A. Sween Company
Hodges, SC
· As a Flex Associate you will be responsible for learning various roles that supports both Operations and Warehouse. You are expected to follow GMP and Standard Work for the roles of a…
Added 11 mins ago
Warehouse and Logistics Analyst
Stellant Systems
Torrance, CA
…Amplifiers. We combine cutting-edge technology with world-class engineering teams to deliver innovative solutions. Together, we form an invincible…
Added 12 mins ago
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P&C Test Engineer
Actalent
Atlanta, GA
- $27 to $35 USD / hour
Use MS Office and engineering software to document work, maintain records, prepare reports, and support planning and analysis.
Added 12 mins ago
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Quality Assurance Specialist
Actalent
Norwell, MA
- $23 to $32.93 USD / hour
Support the effectiveness review of corrective and preventive actions.
Added 12 mins ago
A
Food Quality Technician 3rd Shift
Actalent
Brockton, MA
- $18 to $22 USD / hour
Associate degree in a science-related field with 12 years of experience in an industry or academic setting, or
Added 12 mins ago
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Senior Manufacturing Technician
Actalent
Fall River, MA
- $52,000 to $72,800 USD / year
Manufacturing Technical Associate | Pharmaceutical Manufacturing
Added 12 mins ago
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Buyer
Actalent
Billerica, MA
- $40 to $50 USD / hour
…timely procurement of materials, components, and services to support engineering and manufacturing. This position actively participates in daily production activities, including Gemba walks…
Added 12 mins ago
Assembly Technician
Actalent
Billerica, MA
Job Title: Engineering TechnicianJob DescriptionThe Engineering Technician assembles and wires electrical control boxes and electromechanical prototype units using electrical schematics and…
Added 12 mins ago
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Manufacturing Associate
Actalent
Plainville, MA
- $27 to $28 USD / hour
Manufacturing Associate | Biopharmaceutical Manufacturing
Added 12 mins ago
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Quality Control Microbiologist
Actalent
West Greenwich, RI
- $25 to $35 USD / hour
We are seeking an Associate Quality Control Analyst to support a growing Quality Control team within a regulated manufacturing environment. This individual will perform routine analytical…
Added 12 mins ago
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Quality Control Chemist
Actalent
West Greenwich, RI
- $25 to $35 USD / hour
We are seeking a Quality Control Analyst Associate to support the night-shift QC team within a large biopharmaceutical manufacturing environment. This individual will perform routine…
Added 12 mins ago
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Research Data Associate
Actalent
New York, NY
- $28 USD / hour
…to clinical research by providing direct data and regulatory support for clinical trials, studies, and general research activities under direct supervision. The Research Data Associate…

Actalent

Research Data Associate

New York, NY, United States

$28 USD / hour

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Job details

Pay: $28 USD / hour
Education: Bachelor’s degree
Posting language: English
Posted: Nov 9, 2026

Original job description

Job Title: Research Data AssociateDuration: 12-month contract to hireJob DescriptionThis role offers an exciting opportunity to contribute to clinical research by providing direct data and regulatory support for clinical trials, studies, and general research activities under direct supervision. The Research Data Associate helps ensure that clinical trials remain compliant and progress smoothly through the regulatory process by managing submissions, documentation, and ongoing regulatory requirements for a large portfolio of studies in pediatric hematology and oncology.Responsibilities

Activate and initiate new clinical trials in alignment with regulatory and institutional requirements.
Process protocol amendments and personnel changes, ensuring all updates are accurately documented and submitted.
Coordinate and submit continuing review applications to maintain active study approval.
Maintain regulatory compliance across active studies by tracking and fulfilling all regulatory obligations.
Prepare documentation and materials for study monitoring visits, sponsor visits, and regulatory audits.
Maintain, organize, and update regulatory binders and essential study documents for each trial.
Track study renewals and regulatory deadlines to ensure timely submissions and prevent lapses in approvals.
Communicate directly with the Institutional Review Board (IRB) regarding submissions, amendments, and ongoing study requirements.
Ensure investigator and study staff documentation remains current, including medical licenses, training certifications, CVs, and other supporting regulatory documents.
Support regulatory oversight for approximately 100 active clinical trials at various stages of conduct.
Manage renewals and regulatory submissions for approximately 510 studies per month.
Work with studies spanning multiple phases and disease areas within pediatric hematology and oncology.
Maintain a high level of organization to manage heavy documentation, compliance tracking, and strict deadlines.
Perform primarily computer-based work focused on ongoing regulatory documentation responsibilities.
Operate effectively in a fast-paced environment with a consistent workflow and time-sensitive tasks.

Essential Skills

Experience or strong interest in clinical data handling, data entry, and documentation accuracy.
Understanding or exposure to regulatory documents and regulatory affairs in a clinical research setting.
Ability to manage study paperwork, including IRB submissions, protocol amendments, and continuing reviews.
Strong organizational skills with the ability to track multiple studies, deadlines, and regulatory requirements simultaneously.
High attention to detail when preparing and maintaining regulatory binders and essential study documents.
Effective written and verbal communication skills for direct interaction with the Institutional Review Board and internal study teams.
Comfort working extensively with computer-based systems and electronic documentation.
Ability to work efficiently in a fast-paced, deadline-driven environment.

Additional Skills & Qualifications

Bachelor's degree required.
Recent graduates are encouraged to apply.
Prior exposure to clinical research through internships, research assistant roles, regulatory internships, or academic research is a plus but not required.
Educational background in life sciences, public health, psychology, biology, biomedical sciences, or a related field is preferred.
Strong willingness to learn and grow within the field of clinical research.
Interest in pediatric hematology and oncology research is beneficial.

Work EnvironmentThis position is part of a pediatric hematology and oncology research group that supports clinical studies focused on cancer and blood disorders. The role is fully onsite, based at a research facility in New York, New York. The standard schedule is Monday through Friday, 9:00 a.m. to 5:00 p.m., with a one-hour lunch break, resulting in a 35-hour work week. You will work closely with a collaborative team of coordinators and regulatory staff who are onsite and engaged in supporting a large portfolio of active clinical trials. Most work is computer-based and involves handling regulatory documentation, tracking compliance, and meeting frequent deadlines in a fast-paced environment. This is a 12-month contract-to-hire opportunity, offering the potential to transition into a longer-term role based on performance and organizational needs. Job Type & LocationThis is a Contract position based out of New York, NY. Pay and BenefitsThe pay range for this position is $28.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract position based out of New York, NY. Application DeadlineThis position is anticipated to close on Nov 23, 2026. Workplace TypeThis is a fully onsite position in New York,NY.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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More about this job

Skills

Research
Clinical research
Clinical trials
Regulatory compliance
Documentation
Workflow
Data entry
Regulatory affairs
Organizational skills
Attention to detail
Communication skills
Work efficiently
Biomedical science

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