Clinical Trial Manager or Associate Clinical Trial Manager
Rapport Therapeutics, Boston, MA, United States
When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we’re driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we’re doing this with extraordinary science and awesome people (affectionately called Rapptors).
The role is based in Boston, MA with onsite presence required Monday‑Wednesday.
Your Impact
In this role, you’ll work with our Clinical Operations Leads to help keep trials running smoothly across multiple indications. It’s a hands‑on, high‑impact role on a fun, driven team where you’ll grow fast and make a real difference.
Your Day‑to‑Day
Provide support to the Clinical Operations Lead (COL) in the planning, execution, and oversight of a global phase 3 clinical trial from study start‑up to close‑out.
Support the development, review and tracking of study‑related documents (protocols, ICFs, investigative brochure, monitoring visit reports, etc.) with cross‑functional team collaboration.
Support start‑up activities to accelerate country and site activations.
Oversee CRO and vendors, monitor performance metrics, and ensure timely and high‑quality deliverables.
Track study timelines, enrollment, protocol deviations, data trends, and sample management in partnership with CRO and internal stakeholders.
Maintain and organize trial documentation (e.g., TMF/eTMF oversight, trackers, meeting minutes) ensuring that study documentation is in a continuous state of inspection readiness.
Contribute to inspection readiness activities and ensure compliance with GCP and SOPs.
Help identify and resolve site risks and/or issues to foster positive site relationships.
Coordinate internal team meetings and participate in cross‑functional study meetings.
Proactively communicate study updates with key internal and external stakeholders.
Must‑Haves
Bachelor’s degree preferably in life sciences or healthcare related field.
5+ years of clinical operations experience within the biotech or pharma industry required
Title and level commensurate with experience
Experience managing outsourced global clinical trials across Phase I–III.
Prior involvement in study start‑up activities strongly preferred.
Solid understanding of GCP, ICH guidelines, and the clinical development process.
Experience with clinical trial management systems (CTMS), eTMF, and other operational tools.
Ability to multitask and flex across projects as priorities and deadlines shift.
Highly organized with excellent communication and interpersonal skills.
Strong attention to detail and ability to multitask in a dynamic, fast‑paced setting.
A collaborative team player that takes initiative.
What Makes Rapport Special
Every role has meaning. We’re determined to discover a better way for patients, and you’ll feel the passion from the start.
We are driven to innovate. Exciting science that pushes boundaries and opens new possibilities.
Your perspective matters. Stick your neck out, share your ideas – we work as a team.
We have FUN. We hire smart, dedicated, down‑to‑earth people that you’ll enjoy spending time with.
Leadership that CARES – about you, your growth + development.
We’re bicoastal. Whether you’re in San Diego full‑time or taking advantage of a more hybrid work schedule in Boston – we make the most of our time together.
Competitive benefits. Including unlimited PTO, a lifestyle spending account, commuting reimbursement, and much more!
You get to be YOU! Show up as you are and make every day count.
Your Compensation
We get it. Compensation is an important part of your offer. You shouldn’t be surprised at the end of the recruiting process, and you should know that your offer is fair and equitable. How do we do this? We tell you about our hiring range now – we expect the hiring range for the Associate Clinical Trial Manager is $115,000–$135,000 and for Clinical Trial Manager it is $140,000–$160,000. Our actual offer will reflect a lot of factors including your relevant skills, experience, location, salary market data, and internal equity. In addition to a competitive salary, we also offer a pretty great benefits package. We don’t stop here – if you join Rapport, we go to the next level. We share our full salary ranges for every level across our company.
Hybrid Work Environment
We prioritize in‑person connection with our fellow Rapptors! Our team members come together onsite at our Boston office Monday‑Wednesday to create more opportunities for innovation, collaboration, and connection.
Rapport Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.
CCPA disclosure notice can be found here.
#J-18808-Ljbffr
The role is based in Boston, MA with onsite presence required Monday‑Wednesday.
Your Impact
In this role, you’ll work with our Clinical Operations Leads to help keep trials running smoothly across multiple indications. It’s a hands‑on, high‑impact role on a fun, driven team where you’ll grow fast and make a real difference.
Your Day‑to‑Day
Provide support to the Clinical Operations Lead (COL) in the planning, execution, and oversight of a global phase 3 clinical trial from study start‑up to close‑out.
Support the development, review and tracking of study‑related documents (protocols, ICFs, investigative brochure, monitoring visit reports, etc.) with cross‑functional team collaboration.
Support start‑up activities to accelerate country and site activations.
Oversee CRO and vendors, monitor performance metrics, and ensure timely and high‑quality deliverables.
Track study timelines, enrollment, protocol deviations, data trends, and sample management in partnership with CRO and internal stakeholders.
Maintain and organize trial documentation (e.g., TMF/eTMF oversight, trackers, meeting minutes) ensuring that study documentation is in a continuous state of inspection readiness.
Contribute to inspection readiness activities and ensure compliance with GCP and SOPs.
Help identify and resolve site risks and/or issues to foster positive site relationships.
Coordinate internal team meetings and participate in cross‑functional study meetings.
Proactively communicate study updates with key internal and external stakeholders.
Must‑Haves
Bachelor’s degree preferably in life sciences or healthcare related field.
5+ years of clinical operations experience within the biotech or pharma industry required
Title and level commensurate with experience
Experience managing outsourced global clinical trials across Phase I–III.
Prior involvement in study start‑up activities strongly preferred.
Solid understanding of GCP, ICH guidelines, and the clinical development process.
Experience with clinical trial management systems (CTMS), eTMF, and other operational tools.
Ability to multitask and flex across projects as priorities and deadlines shift.
Highly organized with excellent communication and interpersonal skills.
Strong attention to detail and ability to multitask in a dynamic, fast‑paced setting.
A collaborative team player that takes initiative.
What Makes Rapport Special
Every role has meaning. We’re determined to discover a better way for patients, and you’ll feel the passion from the start.
We are driven to innovate. Exciting science that pushes boundaries and opens new possibilities.
Your perspective matters. Stick your neck out, share your ideas – we work as a team.
We have FUN. We hire smart, dedicated, down‑to‑earth people that you’ll enjoy spending time with.
Leadership that CARES – about you, your growth + development.
We’re bicoastal. Whether you’re in San Diego full‑time or taking advantage of a more hybrid work schedule in Boston – we make the most of our time together.
Competitive benefits. Including unlimited PTO, a lifestyle spending account, commuting reimbursement, and much more!
You get to be YOU! Show up as you are and make every day count.
Your Compensation
We get it. Compensation is an important part of your offer. You shouldn’t be surprised at the end of the recruiting process, and you should know that your offer is fair and equitable. How do we do this? We tell you about our hiring range now – we expect the hiring range for the Associate Clinical Trial Manager is $115,000–$135,000 and for Clinical Trial Manager it is $140,000–$160,000. Our actual offer will reflect a lot of factors including your relevant skills, experience, location, salary market data, and internal equity. In addition to a competitive salary, we also offer a pretty great benefits package. We don’t stop here – if you join Rapport, we go to the next level. We share our full salary ranges for every level across our company.
Hybrid Work Environment
We prioritize in‑person connection with our fellow Rapptors! Our team members come together onsite at our Boston office Monday‑Wednesday to create more opportunities for innovation, collaboration, and connection.
Rapport Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.
CCPA disclosure notice can be found here.
#J-18808-Ljbffr