Top 26 Science Jobs in Calabash Nc

FSP Country Approval Specialist
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Computer literacy
- English
- Mid-level
4d
Global Study Lead - FSP Team
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Office
- Bachelor's degree
- Conflict management
4d
Alligator Adventure animal staff
BAREFOOT ZOOLOGICAL GARDENS LLC —North Myrtle Beach, SC
- Full-time
- Communication skills
- Entry level
Quick Apply
12h
Green Swamp Conservation Technician I
State of North Carolina - North Carolina Wildlife Resources Commission —Brunswick County, NC
- $33,902 - $59,327 a year
- Weekends as needed
- CDL A
- Ability to lift 50 pounds
- Data entry
Meteorologist
Nexstar Broadcasting —Myrtle Beach, SC
- Extended hours
- Bachelor's degree
- Entry level
8d
Senior CRC
AMR Clinical —Myrtle Beach, SC
- Overtime
- Vital signs
- English
- 3 years
- Flexible schedule
Quick Apply
8d
Computational Chemistry Expert - AI trainer
micro1 —United States
- $20 - $60 an hour
- Contract
- Remote
- No experience needed
- Math
- Doctor of Philosophy
- Flexible schedule
Director, Gene Therapy Clinical Science
Rocket Pharmaceuticals —United States
- $206,000 - $270,000 a year
- Full-time
- Nursing
- 11+ years
- Bachelor of Science in Nursing
- Paid holidays
- Health insurance
Computational Biology Expert - AI trainer
micro1 —United States
- $20 - $60 an hour
- Contract
- Remote
- No experience needed
- Analysis skills
- Doctor of Philosophy
- Flexible schedule

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Industrial Account Manager - Chemical Water Treatment Solutions
Water Technologies —Wilmington, NC
A full valid driver's license and willingness to travel (a learner’s permit or G1/G2 class will not qualify). You'll be more than a sales professional – you'll…
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Environmental Specialist I (Temporary - New Hanover)
State of North Carolina - OSHR Temporary Solutions —New Hanover County, NC
Ability to organize and direct moderately complex research or field studies. Bachelor's degree in one of the agricultural, biological, engineering,…
$26 an hour

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Laboratory Technician (Environmentally Assisted Cracking Labs)
EDISON WELDING INSTITUTE INC —Columbus, OH
Three (3) years of experience operating mechanical test equipment. Operate complex, multi-parameter laboratory systems safely in environments involving…
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Product Application Specialist
Crimson Cup —Columbus, OH
Create and maintain tasting tools (scorecards, sensory descriptors, preference questions) and compile results into clear summaries and recommendations.
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FSP Country Approval Specialist

Thermo Fisher Scientific -
North Carolina

Apply Now

Job Details

Full-time
4 days ago

Qualifications

Computer literacy

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you’ll have the opportunity to participate in the management and preparation, review, and coordination of Country Submissions in line with the global submission strategy. As a Country Approval Specialist, you'll play a key role in ensuring that submissions are managed effectively and align with our strategic goals.

What You’ll Do:

Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy.
Provides, under guidance local regulatory strategy advice (MoH &/or EC) to internal clients.
Provides project specific local SIA services and coordination of these projects.
May have contact with investigators for submission related activities.
Key-contact at country level for either Ethical or Regulatory submission-related activities.
Coordinates, under guidance, with internal functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed upon timelines; ensures alignment of submission process for sites and study are aligned to the critical path for site activation.
Achieves PPD’s target cycle times for site.
May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable.
May develop country specific Patient Information Sheet/Informed Consent form documents.
May assist with grant budgets(s) and payment schedules negotiations with sites.
Supports the coordination of feasibility activities, as required, in accordance with agreed timelines.
Entes and maintains trial status information relating to SIA activities onto PPD tracking databases in an accurate and timely manner.
Ensures the local country study files and filing processes are prepared, set up and maintained as per PPD WPDs or applicable client SOPs.
Maintains knowledge of and understand PPD SOPs, Client SOPs/directives, and current regulatory guidelines as applicable to services provided.

Education and Experience Requirements:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).

Previous Contract Research Organization (CRO) experience is highly preferred.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Effective oral and written communication skills
Excellent interpersonal skills
Strong attention to detail and quality of documentation
Good negotiation skills
Good computer skills and the ability to learn appropriate software
Good English language and grammar skills
Basic medical/therapeutic area and medical terminology knowledge
Ability to work in a team environment or independently, under direction, as required
Basic organizational and planning skills
Basic knowledge of all applicable regional / national country regulatory guidelines and EC regulations

Working Conditions and Environment:

Work is performed in an office/ laboratory and/or a clinical environment.
Exposure to biological fluids with potential exposure to infectious organisms.
Exposure to electrical office equipment.
Personal protective equipment required such as protective eyewear, garments and gloves

Apply Now

Refine Your Search

science jobs in calabash nc

FSP Country Approval Specialist

Global Study Lead - FSP Team

Alligator Adventure animal staff

Green Swamp Conservation Technician I

Meteorologist

Senior CRC

Computational Chemistry Expert - AI trainer

Director, Gene Therapy Clinical Science

Computational Biology Expert - AI trainer

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