Doctoral (PharmD or PhD) degree preferred Qualifications * Bachelor's Required. Doctoral (PharmD or PhD) degree preferred * Minimum of 5-7 years of experience in clinical research in the ...
Doctoral (PharmD or PhD) degree preferred Qualifications * Bachelor's Required. Doctoral (PharmD or PhD) degree preferred * Minimum of 5-7 years of experience in clinical research in the ...
Clinical Research Scientist
Madison, NJ ยท On-site
$60/hr
Qualifications MD, PhD, or PharmD: 0 to 3 years with industry experience in clinical development ... hospital or research organization MS: 3 to 5 years of clinical development/clinical trial ...
Clinical Research Scientist
Madison, NJ ยท On-site
$60/hr
Qualifications MD, PhD, or PharmD: 0 to 3 years with industry experience in clinical development ... hospital or research organization MS: 3 to 5 years of clinical development/clinical trial ...
Clinical Research Coordinator
Jacksonville, FL ยท On-site
$21.75 - $29/hr
BSN, PharmD, MD or PhD preferred * 2+ years of work as a clinical research coordinator in an oncology setting * CCRC preferred Compensation and Benefits: * Salary is commensurate with experience and ...
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Clinical Research Coordinator
Jacksonville, FL ยท On-site
$21.75 - $29/hr
BSN, PharmD, MD or PhD preferred * 2+ years of work as a clinical research coordinator in an oncology setting * CCRC preferred Compensation and Benefits: * Salary is commensurate with experience and ...
Title: Clinical Research Scientist Duration: 12 Months (Possibility of Extension) Location ... Doctoral (PharmD or PhD) or MD degree preferred. Additional Information Feel free to forward my ...
Title: Clinical Research Scientist Duration: 12 Months (Possibility of Extension) Location ... Doctoral (PharmD or PhD) or MD degree preferred. Additional Information Feel free to forward my ...
Scientist
West Chester, PA ยท On-site
... โข PharmD (clinical pharmacology background/experience). โข Problem solving skills. โข ... in clinical research (designing/managing clinical studies and Good Clinical Practices). โข ...
Scientist
West Chester, PA ยท On-site
... โข PharmD (clinical pharmacology background/experience). โข Problem solving skills. โข ... in clinical research (designing/managing clinical studies and Good Clinical Practices). โข ...
Clinical Research Scientist
Portsmouth, NH ยท On-site
$125K - $185K/yr
As our new Clinical Research Scientist , you'll play a key role in advancing our global clinical ... Advanced scientific degree (MD, PhD, or PharmD). * Minimum of 2-3 years of combined oncology and/or ...
Clinical Research Scientist
Portsmouth, NH ยท On-site
$125K - $185K/yr
As our new Clinical Research Scientist , you'll play a key role in advancing our global clinical ... Advanced scientific degree (MD, PhD, or PharmD). * Minimum of 2-3 years of combined oncology and/or ...
... address research questions In collaboration with other clinical staff and/or an external CRO ... Doctoral (PharmD or PhD) degree preferred Qualifications BS/MS Additional Information For more ...
... address research questions In collaboration with other clinical staff and/or an external CRO ... Doctoral (PharmD or PhD) degree preferred Qualifications BS/MS Additional Information For more ...
PRN - Clinical Trial PharmD
Houston, TX ยท On-site
$32 - $43.75/hr
The primary purpose of the Clinical Trial PharmD is to provide oversight for investigational drug ... Collaborate with investigators, clinical research coordinators, sponsors, and CROs to support study ...
PRN - Clinical Trial PharmD
Houston, TX ยท On-site
$32 - $43.75/hr
The primary purpose of the Clinical Trial PharmD is to provide oversight for investigational drug ... Collaborate with investigators, clinical research coordinators, sponsors, and CROs to support study ...
Clinical Research Pharmacist
$75 - $85/hr
The Clinical Research Pharmacist (PRN) is responsible for managing and coordinating the ... Doctor of Pharmacy (PharmD) degree required. * Active, unrestricted Pharmacist license in the state ...
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Clinical Research Pharmacist
$75 - $85/hr
The Clinical Research Pharmacist (PRN) is responsible for managing and coordinating the ... Doctor of Pharmacy (PharmD) degree required. * Active, unrestricted Pharmacist license in the state ...
Clinical Research Pharmacist
San Jose, CA ยท On-site
$45 - $60/hr
The Clinical Research Pharmacist (PRN) is responsible for managing and coordinating the ... Doctor of Pharmacy (PharmD) degree required. * Active, unrestricted Pharmacist license in the state ...
Clinical Research Pharmacist
San Jose, CA ยท On-site
$45 - $60/hr
The Clinical Research Pharmacist (PRN) is responsible for managing and coordinating the ... Doctor of Pharmacy (PharmD) degree required. * Active, unrestricted Pharmacist license in the state ...
MD, PhD, or PharmD in a relevant discipline (Oncology, Immunology, Pharmacology, Molecular Biology). * 12+ years oncology clinical research/drug development experience (pharma/biotech/academic/CRO)
MD, PhD, or PharmD in a relevant discipline (Oncology, Immunology, Pharmacology, Molecular Biology). * 12+ years oncology clinical research/drug development experience (pharma/biotech/academic/CRO)
Role Overview The Global Pain Clinical Research Scientist (CRS) provides scientific and clinical ... Advanced degree (PharmD, PhD, DVM, MSN/NP, or related) + 5+ years clinical/pharmaceutical ...
Role Overview The Global Pain Clinical Research Scientist (CRS) provides scientific and clinical ... Advanced degree (PharmD, PhD, DVM, MSN/NP, or related) + 5+ years clinical/pharmaceutical ...
Executive Director, Clinical Research Office
Los Angeles, CA ยท On-site
$181K - $282K/yr
Certification in clinical research coordination (e.g., ACRP/SoCRA - CCRC) and/or experience as a healthcare provider (RN, LPN, PA, PharmD, NP, etc.). * Advanced degree in a relevant field e.g., MHA ...
Executive Director, Clinical Research Office
Los Angeles, CA ยท On-site
$181K - $282K/yr
Certification in clinical research coordination (e.g., ACRP/SoCRA - CCRC) and/or experience as a healthcare provider (RN, LPN, PA, PharmD, NP, etc.). * Advanced degree in a relevant field e.g., MHA ...
As a Director, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging ... PhD, PharmD or other related Advanced Medical Scientific Degree. * Experience in oncology is a must.
As a Director, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging ... PhD, PharmD or other related Advanced Medical Scientific Degree. * Experience in oncology is a must.
As a Director, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging ... PhD, PharmD or other related Advanced Medical Scientific Degree. * Experience in oncology is a must.
As a Director, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging ... PhD, PharmD or other related Advanced Medical Scientific Degree. * Experience in oncology is a must.
Advanced scientific or clinical degree (MD, PharmD, PhD, DNP, or equivalent). * Minimum 10 years of experience in clinical research, clinical development, medical affairs, or evidence generation.
Advanced scientific or clinical degree (MD, PharmD, PhD, DNP, or equivalent). * Minimum 10 years of experience in clinical research, clinical development, medical affairs, or evidence generation.
Advanced scientific or clinical degree (MD, PharmD, PhD, DNP, or equivalent). * Minimum 10 years of experience in clinical research, clinical development, medical affairs, or evidence generation.
Advanced scientific or clinical degree (MD, PharmD, PhD, DNP, or equivalent). * Minimum 10 years of experience in clinical research, clinical development, medical affairs, or evidence generation.
As a Director, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging ... PhD, PharmD or other related Advanced Medical Scientific Degree. Experience in oncology is a must.
As a Director, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging ... PhD, PharmD or other related Advanced Medical Scientific Degree. Experience in oncology is a must.
Clinical Research Associate
North Bethesda, MD ยท On-site
$115K - $135K/yr
Bachelor's degree in a scientific, health-related, or clinical field, or professional healthcare licensure (RN, PharmD, PA, NP, MD, DO, etc.), or equivalent Clinical Research Associate certification.
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Clinical Research Associate
North Bethesda, MD ยท On-site
$115K - $135K/yr
Bachelor's degree in a scientific, health-related, or clinical field, or professional healthcare licensure (RN, PharmD, PA, NP, MD, DO, etc.), or equivalent Clinical Research Associate certification.
Position Overview - Clinical Research Associate As a CRA, you'll manage clinical study activities ... PharmD. * At least 4 plus years of onsite monitoring experience is required. * Previous medical ...
Position Overview - Clinical Research Associate As a CRA, you'll manage clinical study activities ... PharmD. * At least 4 plus years of onsite monitoring experience is required. * Previous medical ...
Pharmd Clinical Research information
See salary details
$13.22 - $15.73
11% of jobs
$15.73 - $18.25
10% of jobs
$19.41 is the 25th percentile. Wages below this are outliers.
$18.25 - $20.76
7% of jobs
$20.76 - $23.27
19% of jobs
The median wage is $23.45 / hr.
$23.27 - $25.79
37% of jobs
$25.79 - $28.30
0% of jobs
$28.30 - $30.81
3% of jobs
$30.81 - $33.33
3% of jobs
$33.33 - $35.84
3% of jobs
$35.84 - $38.35
3% of jobs
$38.35 - $40.87
3% of jobs
$13
$24
$40
How much do pharmd clinical research jobs pay per hour?
What are popular job titles related to Pharmd Clinical Research jobs?
For Pharmd Clinical Research jobs, the most frequently searched job titles are:

Clinical Research Scientist
Woodcliff Lake, NJ โข On-site
Contractor
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 2 days ago
Job description
About LanceSoft:
Headquartered in Herndon, Virginia, LanceSoft is one of the fastest growing IT services Company. We are geographically spread to cover all the 50 states in the US and our global software development centers have the capability and capacity to cater to our global client's requirements in the most efficient manner. We have experienced exponential growth over the last few years and anticipate continuing to do so in the future as well. We have won numerous national, regional and state awards for being one of the fastest growing companies in the US. Our prestigious client base comprises of a number of Fortune 500 companies. LanceSoft dynamic work environment and culture constantly nurtures innovation, strategic thinking, and creativity and is complemented by strict process controls across our delivery centers globally. With attractive compensation packages, positive and productive work environments and challenging assignments to offer, LanceSoft is committed to being the employer of choice. We are committed not only to attracting and hiring top talent in the industry, but also developing and maintaining long-term relationships. LanceSoft recognizes true potential and provides people with the right opportunities. We offer a complete range of benefit packages to our employees which includes but is not limited to paid vacations, holidays, personal days, medical, dental and vision insurance, 401K savings plan, life insurance, disability insurance and many other attractive benefits.
I look forward to work with you and encourage you to visit our website www.LanceSoft.com to learn more about LanceSoft as an organization.
Description
The incumbent is responsible for, but not limited to the following:
Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies
Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator Brochure, etc)
Performs literature search and data analysis to address research questions
In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.)
Assisting in database cleaning, review of study results, and interpretation of results
Adhering to key performance indicators for clinical study development, conduct, and reporting
Individual contributor with specialized knowledge
Presents concepts, facts, and reports and advises on key trends and issues
Troubleshooting routine site inquiries
Work is completed under limited supervision
Supports the planning, execution and reporting of clinical programs/trials
May handle multiple protocols simultaneously
Contributes to risk resolution by escalating and monitoring project risks
Minimum of 5-7 years of experience in clinical research in the pharmaceutical industry
A thorough understanding of clinical research methodology including study design, protocol writing, and CRF preparation is required, as is a knowledge of GCP and local regulatory requirements
Working knowledge of the IND/NDA/ CTD/ MAA process acquired through direct industrial experience preferred
Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area;
Bachelor's Required. Doctoral (PharmD or PhD) degree preferred
- Bachelor's Required. Doctoral (PharmD or PhD) degree preferredย
- Minimum of 5-7 years of experience in clinical research in the pharmaceutical industryย
All your information will be kept confidential according to EEO guidelines.
About LanceSoft
Sourced by ZipRecruiter
Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.
Industry
Recruiting and staffing services
Company size
1,001 - 5,000 Employees
Headquarters location
Herndon, VA, US
Year founded
2000