Clinical Project Manager-Medical Device
- $125,000 - $150,000
- Boston, MA +2
NEW Clinical Project Manager Opportunity-Medical Device experience required!
A bit about us:
We are a well established consulting firm that provides solutions to medical device company, pharmaceuticals and biologics. We are hiring a Clinical Project Manager with medical device experience to join our team!
Why join us?
Opportunity to wear different hats in a small company-lots of growth!
People management if interested
Strong benefits and compensation package
Opportunity to work in multiple therapeutic and diagnostic areas
People management if interested
Strong benefits and compensation package
Opportunity to work in multiple therapeutic and diagnostic areas
Job Details
Job Details:
We are seeking a Clinical Project Manager with Medical Device experience to join our team. This is a unique opportunity to play a pivotal role in the development and implementation of clinical strategies for our innovative medical devices. The successful candidate will be responsible for overseeing clinical trials, managing investigators, and ensuring the integrity of clinical data.
Responsibilities:
As a Clinical Project Manager, you will:
1. Assist with managing and overseeing aspects of clinical trials, from planning to implementation, ensuring compliance with protocols, regulatory requirements, and clinical objectives.
2. Develop and maintain strong relationships with investigators, site staff, and vendors, fostering effective communication and collaboration.
3. Lead the design and review of study documents, including protocols, case report forms, and informed consent forms.
4. Oversee the collection, analysis, and interpretation of clinical data, ensuring accuracy and consistency.
5. Identify, evaluate, and manage potential risks and issues that could impact the successful execution of clinical trials.
6. Collaborate with cross-functional teams, including regulatory affairs, quality assurance, and product development, to ensure alignment and integration of clinical strategies.
7. Prepare and present regular updates and reports on trial progress, costs, and issues to senior management.
Qualifications:
The ideal candidate will have:
1. A Bachelor's degree in Life Sciences, Nursing, or a related field. An advanced degree is preferred.
2. A minimum of 5 years of experience in clinical project management, preferably within the medical device industry.
3. Proven experience managing investigators and overseeing clinical data.
4. Strong knowledge of Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable regulatory requirements.
5. Excellent leadership and team management skills, with the ability to motivate and guide teams to achieve project goals.
6. Exceptional communication and interpersonal skills, with the ability to build strong relationships with internal and external stakeholders.
7. Strong analytical and problem-solving skills, with the ability to make critical decisions under pressure.
8. Proficiency in using clinical trial management systems and other relevant software.
9. Willingness to travel as needed to oversee clinical sites and attend investigator meetings.
This is a fantastic opportunity for a seasoned Clinical Project Manager to contribute to the advancement of medical science and improve patient outcomes. If you are passionate about clinical research and eager to make a significant impact in the medical device industry, we would love to hear from you.
We are seeking a Clinical Project Manager with Medical Device experience to join our team. This is a unique opportunity to play a pivotal role in the development and implementation of clinical strategies for our innovative medical devices. The successful candidate will be responsible for overseeing clinical trials, managing investigators, and ensuring the integrity of clinical data.
Responsibilities:
As a Clinical Project Manager, you will:
1. Assist with managing and overseeing aspects of clinical trials, from planning to implementation, ensuring compliance with protocols, regulatory requirements, and clinical objectives.
2. Develop and maintain strong relationships with investigators, site staff, and vendors, fostering effective communication and collaboration.
3. Lead the design and review of study documents, including protocols, case report forms, and informed consent forms.
4. Oversee the collection, analysis, and interpretation of clinical data, ensuring accuracy and consistency.
5. Identify, evaluate, and manage potential risks and issues that could impact the successful execution of clinical trials.
6. Collaborate with cross-functional teams, including regulatory affairs, quality assurance, and product development, to ensure alignment and integration of clinical strategies.
7. Prepare and present regular updates and reports on trial progress, costs, and issues to senior management.
Qualifications:
The ideal candidate will have:
1. A Bachelor's degree in Life Sciences, Nursing, or a related field. An advanced degree is preferred.
2. A minimum of 5 years of experience in clinical project management, preferably within the medical device industry.
3. Proven experience managing investigators and overseeing clinical data.
4. Strong knowledge of Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable regulatory requirements.
5. Excellent leadership and team management skills, with the ability to motivate and guide teams to achieve project goals.
6. Exceptional communication and interpersonal skills, with the ability to build strong relationships with internal and external stakeholders.
7. Strong analytical and problem-solving skills, with the ability to make critical decisions under pressure.
8. Proficiency in using clinical trial management systems and other relevant software.
9. Willingness to travel as needed to oversee clinical sites and attend investigator meetings.
This is a fantastic opportunity for a seasoned Clinical Project Manager to contribute to the advancement of medical science and improve patient outcomes. If you are passionate about clinical research and eager to make a significant impact in the medical device industry, we would love to hear from you.