Minimum of 5 years working for a Contract Research Organization (CRO), Life Sciences technology company or Pharmaceutical / Biotech organization is required * Previous experience as a CRA, CTM, or in ...
Quick apply
Minimum of 5 years working for a Contract Research Organization (CRO), Life Sciences technology company or Pharmaceutical / Biotech organization is required * Previous experience as a CRA, CTM, or in ...
Quick apply
Minimum of 5 years working for a Contract Research Organization (CRO), Life Sciences technology company or Pharmaceutical / Biotech organization is required * Previous experience as a CRA, CTM, or in ...
Raleigh, NC · On-site +1
Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope ... As our US Clinical Operations team continues to grow, we're looking for a Senior CRA who is ...
Raleigh, NC · On-site +1
Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope ... As our US Clinical Operations team continues to grow, we're looking for a Senior CRA who is ...
Relevant experience includes monitoring as a CRA or working as a study coordinator or clinician ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We ...
Relevant experience includes monitoring as a CRA or working as a study coordinator or clinician ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ... Support CRA and team training on therapeutic areas and study-specific needs * Foster collaboration ...
$11.68 - $16.78
0% of jobs
$16.78 - $21.88
8% of jobs
$21.88 - $26.98
13% of jobs
$28.34 is the 25th percentile. Wages below this are outliers.
$26.98 - $32.08
15% of jobs
$32.08 - $37.17
13% of jobs
The median wage is $37.94 / hr.
$37.17 - $42.27
11% of jobs
$42.27 - $47.37
12% of jobs
$49.17 is the 75th percentile. Wages above this are outliers.
$47.37 - $52.47
13% of jobs
$52.47 - $57.57
14% of jobs
$57.57 - $62.66
2% of jobs
$62.66 - $67.76
1% of jobs
$11
$39
$67
A contract clinical research associate (contract CRA) is a temporary position in which you manage clinical trials and scientific research projects. As a contractor, you work temporarily on a contract that typically lasts for the duration of the project. Clinical research associates work in the pharmaceutical industry to ensure the safety and effectiveness of medication or vaccines. You can also work on studies for biotech companies and projects that perform analysis on surgical procedures or treatments. Your duties focus on planning the trial, defining the parameters, ensuring the safety of participants, and making sure the project meets all regulations and requirements.

Full-time
Medical, Retirement, PTO
Posted 5 days ago
Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation.
Job Title: Director, Business Development
Location: East Coast US
Function: Commercial
The Director, Business Development position is a strategic leader responsible for the overall health, growth, and success of Siteros commercial eClinical and Clinical services.This role involves building and nurturing long term client relationships, executing strategic marketing plans, leading and mentoring account teams, and driving revenue growth through net-new logo generation.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
EDUCATION AND EXPERIENCE:
COMPENSATION & BENEFITS:
$150,000-175,000 salary plus commission
Salary is commensurate on proven experience with a CRO
Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, Variable commission pay, paid time off, and healthcare and retirement benefits.
EMPLOYMENT TYPE:
Full Time, Permanent
COMMITMENTS:
DISCLAIMER:
Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law
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Scientific research and development services
11 - 50 Employees
Miami, FL, US
1999