Top 62 Clinical trial coordinator Jobs in Philadelphia Pa

Clinical Trial Coordinator I/II FSP
Thermo Fisher Scientific —Philadelphia, PA
- $20 - $27 an hour
- Full-time
- Microsoft Word
- Computer literacy
- Mid-level
- Commuter assistance
- Paid parental leave
1d
Clinical Research Coordinator
Thomas Jefferson University and Hospitals —Philadelphia, PA
- Full-time
- Mid-level
- High school diploma or GED
- Ability to lift 50 pounds
- AD&D insurance
- Disability insurance
Clinical Research Coordinator I - Behavioral Health
Children’s Hospital of Philadelphia —Philadelphia, PA
- $53,000 - $66,300 a year
- Full-time
- HIPAA
- High school diploma or GED
- Bachelor's degree
Quick Apply
4d
Coordinator, Clinical Research
Shriners Hospitals for Children —Philadelphia, PA
- $26.58 - $39.86 an hour
- Full-time
- 18 years or older
- Spanish
- English
Quick Apply
5d
Clinical Research Coordinator I - Plastic Surgery
Children’s Hospital of Philadelphia —Philadelphia, PA
- $53,000 - $66,300 a year
- Full-time
- Surgery
- HIPAA
- Mid-level
Quick Apply
Clinical Research Coordinator A
University of Pennsylvania —Philadelphia, PA
- $46,500 a year
- Full-time
- Background check
- Bachelor of Science
- HIPAA
- Health insurance
- Dental insurance
Clinical Research Coordinator I - Profound Autism Research Study
Children’s Hospital of Philadelphia —Philadelphia, PA
- $53,000 - $66,300 a year
- Full-time
- HIPAA
- High school diploma or GED
- Bachelor's degree
Quick Apply
Clinical Research Coordinator I - Cardiology
Children’s Hospital of Philadelphia —Philadelphia, PA
- $53,000 - $66,300 a year
- Full-time
- HIPAA
- Mid-level
- High school diploma or GED
Quick Apply
11d
Clinical Research Coordinator I - Rheumatology
Children’s Hospital of Philadelphia —Philadelphia, PA
- $53,000 - $66,300 a year
- Full-time
- HIPAA
- High school diploma or GED
- Bachelor's degree
Quick Apply
11d
Clinical Research Coordinator (Pulmonary Medicine)
Thomas Jefferson University and Hospitals —Philadelphia, PA
- Full-time
- Mid-level
- Master's degree
- High school diploma or GED
- AD&D insurance
- Disability insurance
Clinical Research Coordinator A - Community Canvasser (Hybrid Eligible)(Department of Dermatology)
University of Pennsylvania —Philadelphia, PA
- $47,313 - $49,554 a year
- Full-time
- Hybrid work
- Background check
- Spanish
- Mid-level
- Health insurance
- Dental insurance
Temporary Data Analyst and Coordinator
Drexel University —Philadelphia, PA
- Part-time
- Hybrid work
- Mid-level
- Master's degree
- 1 year
11d
Clinical Research Coordinator
Temple University —Philadelphia, PA
- $50,000 - $55,000 a year
- Weekends as needed
- Mid-level
- 3 years
- University
- Paid holidays
- Health insurance
11d
Clinical Research Coordinator B
University of Pennsylvania —Philadelphia, PA
- $53,418 - $58,059 a year
- Full-time
- Background check
- Bachelor of Science
- Writing skills
- Health insurance
- Dental insurance
3d
Clinical Research Coordinator (OB-GYNE)
Thomas Jefferson University and Hospitals —Philadelphia, PA
- Full-time
- Mid-level
- Master's degree
- High school diploma or GED
- AD&D insurance
- Disability insurance
Clinical Research Coordinator
Flourish Research —Philadelphia, PA
- $25 - $36 a year
- Full-time
- Vital signs
- HIPAA
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Program Coordinator (Department of Family Medicine and Community Health)
University of Pennsylvania —Philadelphia, PA
- $24.21 - $31.00 an hour
- Full-time
- Background check
- Mid-level
- Clinic
- Health insurance
- Dental insurance
Clinical Research Coordinator B/C
University of Pennsylvania —Philadelphia, PA
- $53,418 - $63,085 a year
- Full-time
- Hybrid work
- Background check
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Clinical Research Coordinator A/B/C
University of Pennsylvania —Philadelphia, PA
- $47,313 - $67,046 a year
- Full-time
- Background check
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Clinical Research Coord II
Main Line Health —Wynnewood, PA
- Part-time
- Hospital
- Bachelor of Science
- English
- Free parking
- Tuition reimbursement

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Clinical Trial Coordinator I/II FSP

Thermo Fisher Scientific -
Philadelphia, PA

Apply Now

Job Details

Full-time
$20 - $27 an hour
1 day ago

Benefits

Commuter assistance
Paid parental leave
Caregiver leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
Life insurance

Qualifications

Employee relationship building

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Trial Coordinator I/II FSP – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotech’s, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

Role-related skills

Excellent technical/IT skills. Able to understand the impact of technology on studies and to use and develop computer skills while making appropriate use of Client systems/software
Knowledge of relevant operational procedures, systems and quality guidelines regarding clinical studies
Able to work independently as well as in a team.
Professional attitude with good customer focus (internal and external)

Role Responsibilities

Maintain up to date participating center’s information (including all contact details, contracts and reports).
Responsible for preparing the Investigator and Sponsor files with essential documents for the initiation of sites participating in clinical studies. Assist Client study staff with maintaining the sponsor files during the life of the study. Responsible for archiving at the end of study in accordance with relevant Client SOPs, policies and local regulatory requirements.
Input and oversee Client clinical study tracking systems
Proactively identifies issues and raises them to Client study staff to take necessary corrective action to ensure smooth and rapid progress of studies.
Assist in the planning, logistics and preparation of local Investigator meetings (travel arrangements, assist with preparation and distribution of study related presentation material etc.)
Responsible for working with the Client Study staff for the management of study materials, non-IMP and IMP supplies - distribution, ordering, tracking, storage, reconciliation and destruction using external vendor. Details of destruction to be filed.
As an active participant of clinical study teams, engage in local study meetings during the life of the study to obtain general knowledge about the study and be responsible for given tasks. Assist Client study staff with study related activities such as:
- organizing study meetings and scheduling travel,
- producing minutes for study-related meetings,
- assembling training and study materials,
- updating contact details,
- maintaining study documentation,
- assisting in the preparation of documents and other tasks as required.
Knowledgeable of Client systems
Keep up to date with all the changes/required knowledge on ICH GCP, Client written standards and attending appropriate training sessions.
May be responsible for supporting multiple studies simultaneously and must prioritize appropriately to meet business needs to ensure delivery of results
Requirement to communicate and work effectively with medical staff/physicians/scientists who are often senior within their field, being mindful of their standing within the medical and/or research community.

Education and Experience:

For CTC I position:

High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
Bachelor's degree preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1+ years).

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.

For CTC II position:

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

Knowledge, Skills and Abilities:

Ability to work in a team or independently, as required
Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country
Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non clinical/clinical aspects of project implementation, execution and closeout
Excellent English language and grammar skills and proficient local language skills as needed
Good presentation skills
Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
Ability to successfully complete the organizations clinical training program
Self-motivated, positive attitude with effective strong interpersonal skills
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Excellent interpersonal skills
Strong attention to detail and quality of documentation
Good negotiation skills
Good computer skills and the ability to learn appropriate software
Fluency in local language as well as a good command of the 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 local health systems
Ability to attain and maintain a working knowledge of GCP and applicable SOPs
Excellent customer focus
Proven flexibility and adaptability
Ability to work in a matrix environment
A proven relationship builder
An independent thinker
Ability to manage risk and perform risk escalation appropriately

Compensation and Benefits

The hourly pay range estimated for this position based in North Carolina is $20.00–$27.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

This job posting is for multiple levels:

The salary range estimated for the second level is: $22.00–$27.00

Apply Now

Refine Your Search

clinical trial coordinator jobs in philadelphia pa

Clinical Trial Coordinator I/II FSP

Clinical Research Coordinator

Clinical Research Coordinator I - Behavioral Health

Coordinator, Clinical Research

Clinical Research Coordinator I - Plastic Surgery

Clinical Research Coordinator A

Clinical Research Coordinator I - Profound Autism Research Study

Clinical Research Coordinator I - Cardiology

Clinical Research Coordinator I - Rheumatology

Clinical Research Coordinator (Pulmonary Medicine)

Clinical Research Coordinator A - Community Canvasser (Hybrid Eligible)(Department of Dermatology)

Temporary Data Analyst and Coordinator

Clinical Research Coordinator

Clinical Research Coordinator B

Clinical Research Coordinator (OB-GYNE)

Clinical Research Coordinator

Program Coordinator (Department of Family Medicine and Community Health)

Clinical Research Coordinator B/C

Clinical Research Coordinator A/B/C

Clinical Research Coord II

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