Sr. Clinical Research Associate
SRCRAThis Jobot Job is hosted by:
Audrey BlockAre you a fit? Easy Apply now by clicking the Apply Now button and sending us your resume.
Salary:
$120,000 - $135,000 per yearA bit about us:
We are a well established consulting firm that provides solutions to medical device company, pharmaceuticals and biologics.
Why join us?Opportunity to wear different hats in a small company-lots of growth!Strong benefits and compensation packageOpportunity to work in multiple therapeutic and diagnostic areasJob DetailsJob Details:
Are you passionate about making a significant contribution to the world of science? We are seeking a dedicated and dynamic full time SrClinical Research Associate (CRA) to join our teamThe successful candidate will play a pivotal role in the execution of clinical trials, ensuring the integrity of data and adherence to regulatory guidelinesThis role offers a fantastic opportunity to work at the forefront of scientific research, working with leading biotechnology, pharmaceutical, and medical device companies
Responsibilities:
As a SrCRA, your primary responsibilities will include:
Conducting site visits to assess protocol and regulatory compliance, reviewing Case Report Forms (CRFs), and communicating findings with site staff.
Collaborating with the clinical trial team to develop trial protocols, data collection systems, and final reports.
Ensuring study activities align with Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
Coordinating with the clinical trial sites to ensure timely initiation, monitoring, and completion of clinical trials.
Reviewing and reporting on the progress of studies, including site monitoring reports and enrollment status.
Participating in the preparation of regulatory submissions (IND, NDA).
Facilitating communication between clinical sites, laboratories, and vendors to ensure the smooth running of the trial.
Assisting in the development and implementation of patient recruitment strategies.
Qualifications:
To be considered for this exciting opportunity, you will need:
Bachelor's degree in a scientific or health-related field.
Minimum 3 years of experience as a Clinical Research Associate or in a similar role within the biotechnology, pharmaceutical, or medical device industry.
Proven experience in clinical trials, including site monitoring, study maintenance, and report writing.
Familiarity with regulatory guidelines such as IND and NDA submissions and Good Clinical Practice (GCP).
Excellent communication and interpersonal skills, with the ability to build strong relationships with trial site staff and internal team members.
Strong organizational skills, with the ability to manage multiple projects and meet deadlines.
Willingness to travel as required for site visits, around 50% or so Join us and contribute to advancing scientific knowledge and improving patient outcomesWe offer a competitive compensation package and a collaborative, innovative work environmentIf you have a passion for science and a commitment to excellence, we would love to hear from you.
Interested in hearing more? Easy Apply now by clicking the Apply Now button.
Recommended Skills Biotechnology Case Report Forms Clinical Research Clinical Trials Clinical Works Communication Apply to this job.
Think you're the perfect candidate? Apply Now Estimated Salary: $20 to $28 per hour based on qualifications.
Audrey BlockAre you a fit? Easy Apply now by clicking the Apply Now button and sending us your resume.
Salary:
$120,000 - $135,000 per yearA bit about us:
We are a well established consulting firm that provides solutions to medical device company, pharmaceuticals and biologics.
Why join us?Opportunity to wear different hats in a small company-lots of growth!Strong benefits and compensation packageOpportunity to work in multiple therapeutic and diagnostic areasJob DetailsJob Details:
Are you passionate about making a significant contribution to the world of science? We are seeking a dedicated and dynamic full time SrClinical Research Associate (CRA) to join our teamThe successful candidate will play a pivotal role in the execution of clinical trials, ensuring the integrity of data and adherence to regulatory guidelinesThis role offers a fantastic opportunity to work at the forefront of scientific research, working with leading biotechnology, pharmaceutical, and medical device companies
Responsibilities:
As a SrCRA, your primary responsibilities will include:
Conducting site visits to assess protocol and regulatory compliance, reviewing Case Report Forms (CRFs), and communicating findings with site staff.
Collaborating with the clinical trial team to develop trial protocols, data collection systems, and final reports.
Ensuring study activities align with Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
Coordinating with the clinical trial sites to ensure timely initiation, monitoring, and completion of clinical trials.
Reviewing and reporting on the progress of studies, including site monitoring reports and enrollment status.
Participating in the preparation of regulatory submissions (IND, NDA).
Facilitating communication between clinical sites, laboratories, and vendors to ensure the smooth running of the trial.
Assisting in the development and implementation of patient recruitment strategies.
Qualifications:
To be considered for this exciting opportunity, you will need:
Bachelor's degree in a scientific or health-related field.
Minimum 3 years of experience as a Clinical Research Associate or in a similar role within the biotechnology, pharmaceutical, or medical device industry.
Proven experience in clinical trials, including site monitoring, study maintenance, and report writing.
Familiarity with regulatory guidelines such as IND and NDA submissions and Good Clinical Practice (GCP).
Excellent communication and interpersonal skills, with the ability to build strong relationships with trial site staff and internal team members.
Strong organizational skills, with the ability to manage multiple projects and meet deadlines.
Willingness to travel as required for site visits, around 50% or so Join us and contribute to advancing scientific knowledge and improving patient outcomesWe offer a competitive compensation package and a collaborative, innovative work environmentIf you have a passion for science and a commitment to excellence, we would love to hear from you.
Interested in hearing more? Easy Apply now by clicking the Apply Now button.
Recommended Skills Biotechnology Case Report Forms Clinical Research Clinical Trials Clinical Works Communication Apply to this job.
Think you're the perfect candidate? Apply Now Estimated Salary: $20 to $28 per hour based on qualifications.
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